heck反应的综述

Tetrahedron report number 743

Non-conventional methodologies for transition-metal catalysed

carbon–carbon coupling:a critical overview.

Part 1:The Heck reaction

Francisco Alonso,a,*Irina P.Beletskaya b,*and Miguel Yus a,*

a

Departamento de Qu?

′mica Orga ′nica,Facultad de Ciencias and Instituto de S?′ntesis Orga ′nica (ISO),Universidad de Alicante,Apdo.99,E-03080Alicante,Spain

b

Department of Chemistry,Lomonosov Moscow State University,Vorob’evy Gory,119992Moscow,Russia

Received 10August 2005Available online 29September 2005

Contents

1.

General introduction ..........................................................117721.1.Substrates..............................................................117731.2.Catalytic systems ........................................................117731.3.Solvents ...............................................................

117741.3.1.Supercritical ?uids (SCFs)...........................................117741.3.2.Ionic liquids (ILs)..................................................117741.3.3.Fluorous media ...................................................117751.3.4.Aqueous solvents ..................................................117751.4.Reaction conditions ......................................................

117751.4.1.Physical activation .................................................

117761.4.1.1.Microwave ...............................................117761.4.1.2.Ultrasound ................................................117761.4.1.3.High pressure .............................................

117761.4.2.Physicochemical activation ...........................................

11776

0040–4020/$-see front matter q 2005Elsevier Ltd.All rights reserved.

doi:10.1016/j.tet.2005.08.054

Tetrahedron 61(2005)11771–11835

Keywords :Heck reaction;Supercritical ?uids;Ionic liquids;Fluorous media;Aqueous solvents;Microwave;Ultrasound;High pressure;Nano?ltration;Microreactors;Ball-milling conditions.

Abbreviations :A,ampere;AAEMA,deprotonated form of 2-(acetoacetoxy)ethyl methacrylate;acac,acetylacetonate;Ad,adamantyl;A336,tricaprylmethylammonium chloride;atm,atmosphere;bbim,1,3-di-n -butylimidazolium;b ,block copolymer;bmim,1-butyl-3-methylimidazolium;BINAP,2,20-bis(diphenylphosphino)-1,10-binaphthyl;Boc,tert -butoxycarbonyl;BTF,benzotri?uoride (a ,a ,a -tri?uorotoluene);Cbz,benzyloxycarbonyl;co ,copolymer;COD,1,5-cyclooctadiene;Cy,cyclohexyl;DAB,1,4-diaminobutane;dba,dibenzylideneacetone;DBU,1,8-diazabicyclo[5.4.0]undec-7-ene;DEA,N ,N -diethylacetamide;DEC,dendrimer-encapsulated catalyst;dendr,dendrimer;DIPEA,diisopropylethylamine;DMA,N ,N -dimethylacetamide;DMF,dimethylformamide;DMG,N ,N -dimethylglycine;dppp,1,3-diphenylphosphinopropane;EDG,electron-donating group;EWG,electron-withdrawing group;Fc,ferrocenyl;F-dppp,?uorous-tagged 1,3-bis(diphenylphosphino)propane;HDAPS,N -hexadecyl-N ,N -dimethyl-3-ammonio-2-propanesulfonate;Hex,hexyl;IL,ionic liquid;LDH,layered double hydroxide;M,metal;MCM-41,hexagonally packed mesoporous molecular sieves;MW,microwave;Nf,nona?ate (nona?uoro-n -butane-1-sulfonyl);NMP,N -methylpyrrolidinone;P c ,critical pressure;PAMAM,poly(amidoamine);PEG,poly(ethylene glycol);pmim,1-n -pentyl-3-methylimidazolium;PNIPAM,poly(N -isopropylacrylamide);PNP,p -nitrophenyl;PS,polystyrene;Py,pyridyl;RCM,ring-closing metathesis;ROMP,ring-opening metathesis polymerisation;rt,room temperature;SAPO,silico aluminophosphate;sc,supercritical;SCF,supercritical ?uid;SCM,shell cross-linked micelles;SDS,sodium dodecyl sulfate;TBAA,tetra-n -butyl ammonium acetate;TBAB,tetra-n -butyl ammonium bromide;TBAC,tetra-n -butyl ammonium chloride;TBAF,tetra-n -butyl ammonium ?uoride;TEAC,tetraethylammonium chloride;Tf,tri?uoromethanesulfonyl;TPPDS,bis(p -sulfonatophenyl)phenylphosphane dipotassium salt;Na-TPPMS,mono(m -sulfonatophenyl)diphenylphosphane monosodium salt;m -TPPTC,tris(m -carboxyphenyl)phosphane trilithium salt;TPPTS,tris(m -sulfonatophenyl)phosphane trisodium salt;TXPTS,tris(4,6-dimethyl-3-sulfonatophenyl)phosphane trisodium salt;T c ,critical temperature;THF,tetrahydrofuran;THP,tetrahydropyranyl;TFA,tri?uoroacetic acid;Tol,tolyl;TOF,turnover frequency (mol of product per mol of catalyst h K 1);TON,turnover number (mol of product per mol of catalyst);Ts,p -toluenesulfonyl;ttmpp,tris-(2,4,5-trimethoxyphenyl)phosphane;wt,weight;XAFS,X-ray absorption ?ne structure.

*Corresponding authors.Tel./fax:C 34965903549;(F.A.;M.Y.);fax:C 7959381844;(I.P.B.);e-mail addresses:falonso@ua.es;beletska@org.chem.msu.ru;yus@ua.es

1.4.2.1.Micellar solutions (11776)

1.4.2.2.Microemulsions (11777)

1.4.3.Electrochemical activation (11777)

1.5.Miscellaneous non-conventional techniques (11777)

1.5.1.Nano?ltration (11777)

1.5.2.Microreactors (11777)

1.5.3.Ball-milling conditions (11778)

2.Objectives and organisation (11778)

3.Introduction to the Heck reaction (11778)

4.Substrates (11778)

4.1.Alternative arylating agents (11778)

4.2.Supported substrates (11782)

5.Catalytic systems (11785)

5.1.Ligands:ligand-free catalytic systems (11785)

5.2.Catalysts:supported catalysts (11787)

5.2.1.Carbon (11787)

5.2.2.Metal oxides and other inorganic materials (11788)

5.2.3.Clays,zeolites and molecular sieves (11795)

5.2.4.Polymers (11798)

5.2.5.Dendrimeric systems (11803)

6.Solvents (11806)

6.1.Supercritical?uids (11806)

6.2.Ionic liquids (11808)

6.3.Fluorous media (11814)

6.4.Aqueous solvents (11817)

7.Reaction conditions (11820)

7.1.Physical activation (11820)

7.1.1.Microwave (11820)

7.1.2.Ultrasound (11822)

7.1.3.High pressure (11822)

7.2.Physicochemical activation (11823)

7.2.1.Micellar solutions (11823)

7.2.2.Electrochemical activation (11824)

8.Miscellaneous non-conventional techniques (11824)

8.1.Nano?ltration (11824)

8.2.Microreactors (11825)

8.3.Ball-milling conditions (11826)

9.General conclusions (11826)

References and notes (11826)

Biographical sketches (11835)

1.General introduction

The formation of carbon–carbon bonds is a fundamental reaction in organic synthesis the ef?ciency of which has interested organic chemists for a long time ago.Aryl–aryl bond formation has been known for more than a century and was one of the?rst reactions involving a transition metal.1 Modern synthetic chemistry is also sustained by the use of transition-metal catalysts as powerful tools for carbon–carbon bond-forming processes.2Among these, carbon–carbon coupling reactions through the activation of carbon–hydrogen bonds,3as well as addition reactions,4 have experienced an increasing interest in the preparation of molecules,the access to which is not so straightforward using other methodologies.On the other hand,the transition-metal catalysed carbon–carbon bond formation developed in the1970s represented a milestone in synthetic organic chemistry that allowed the cross coupling of substrates in ways that would have previously been thought impossible.5This protocol has been substantially improved and expanded over the past30years,providing an indispensable and simple methodology for preparative organic chemists(Scheme1

).

Scheme1.

F.Alonso et al./Tetrahedron61(2005)11771–11835 11772

In spite of the fact that it would seem that most of the research on developing carbon–carbon coupling strategies has been done,some new challenges on this topic have emerged in the narrow boundary between the20th and21st century.A new mentality of the organic chemist is focussed on the design of new tendencies and methodologies able to make the already known chemical transformations simpler, faster,cheaper,greener and in general,more ef?cient processes.In particular,increasing attention has been paid to the‘green chemistry’of these processes,this concept being understood as the set of principles6that reduce or eliminate the use or generation of hazardous substances.7 The idea of atom-economical reactions may be also a useful concept in helping to promote thinking in the direction of sustainable chemistry.8In order to achieve all the goals mentioned above,several valuable and distinctive tech-niques,9which do not?nd daily use in the laboratory,can be applied by the organic chemist to operate at different levels including(a)the type of substrates,(b)the catalyst,(c)the solvent,(d)the reaction conditions,(e)the separation techniques and(d)the reaction vessel.An introductory commentary to remark the importance of any of these parameters follows.

1.1.Substrates

The majority of studies of metal-catalysed cross-coupling reactions involve a halide or sulfonate as the electrophile and an organometallic reagent as the nucleophile in which the carbon atoms to be coupled are all sp2-hybridized.There is,however,a substantial need for the development of successful cross-coupling reactions involving either alkyl halides or https://www.wendangku.net/doc/7e2513454.html,anic halides also take part in Heck-type reactions.On the other hand,all these processes have in common some lack of atom economy,8since the corresponding inorganic salts are obtained and require proper isolation and treatment.

In the past decade,there have been developments in palladium-catalysed coupling systems for Heck,Suzuki, Stille and Sonogashira reactions among others,as a consequence of the great interest in the development of coupling partners that are both more economical and readily accessible.In spite of the fact that organoboranes and organostannanes have been the reagents of choice for some of these reactions,there are still some drawbacks in their use:certain organostannanes such as the trimethyltins, Me3SnX and their by-products are toxic,whereas organo-boranes have a lack of stability,particularly alkyl-and alkynylboranes.

Consequently,the search for novel substrates for the cross-coupling reactions has been the focus of much attention,for example,carboxylic acids,anhydrides and esters,as well as sulfonium salts,thiol esters and thioethers,have emerged as interesting alternatives to aryl halides.10In particular, carboxylic acids do not generate large amounts of waste and they work in the absence of phosphane ligands.There is, however,no general advantage in terms of atom economy and their generation in not always readily accessible, producing stoichiometric amounts of salts as by-products. The Stille,Suzuki and Kumada reactions with alkyl and aryl ?uorides is a recent and promising research area leading to the cross-coupled products under generally mild reaction conditions.11The stability of vinylic tellurides has also been used in palladium-catalysed cross-coupling reactions for the preparation of stereochemically de?ned enynes and enediynes.The fact that these reagents work in the presence of sensitive functional groups and under mild reaction conditions makes them interesting substitutes for vinylic halides and tri?ates.12

On the other hand,potassium tri?uoro(organo)borates are promising alternatives to the use of the known organo-boronic acids,exhibiting higher reactivity and exceptional stability.13Germanium reagents have been recently used in cross-coupling reactions,14exhibiting intermediate reactivity between that of organotin15and organosilicon compounds,16avoiding the toxicity of certain organotin reagents and being more reactive than silicon.

In recent years,an increasing interest has been shown in the possibility of anchoring the substrates to a solid support, facilitating their use in automated parallel synthesis in a combinatorial manner.The main advantages of these solid-phase transformations are the avoidance of tedious workup procedures,the quasi high-dilution effect(high yields by employing an excess of reagent),amenability to automatisation and the non-interference of various functionalities in the building blocks on a solid support.17 1.2.Catalytic systems

The form in which the catalyst is present in the reaction media is fundamental to drive the reaction in an effective manner.A wide range of possibilities can be explored, depending on the different combinations of the components of the catalytic system,for example,the catalyst can be present as nanoparticles,ligandless,unsupported, supported,etc.

Transition-metal nanoparticles have attracted a great deal of attention during the last10years as catalytic systems with great potential,due to the large surface area of the particles. It has been suggested that metal colloids are very ef?cient catalysts because of the ratio of atoms remaining at the surface.In fact,these catalysts are microhetereogenous systems bearing nanoparticles.The application of transition-metal nanoparticles to the formation of carbon–carbon bonds is still,however,in its infancy.18

Recent interest in the development of environmentally benign syntheses and in minimising the cost of the precious metal catalysts has led to the development of polymer-bound metal catalysts for the carbon–carbon coupling reaction that maintain high activity and selectivity.The supported complexes can be recovered from the reaction mixtures,they do not contaminate the product solution and they can be recycled and used for the rapid production of compound libraries.Often,however,there is metal leaching during the course of the reaction and they are often not recyclable.As a result,many efforts have been focussed on the development of new ligand-derivatised polymeric supports for the attachment of metals and on the design of new methods to increase both the activity and the selectivity.19In particular,dendrimers as soluble supports

F.Alonso et al./Tetrahedron61(2005)11771–1183511773

have recently attracted much attention in homogeneous catalysis,since these well-de?ned macromolecular struc-tures enable the construction of precisely controlled catalyst structures.Moreover,the globular shapes of the higher generations of dendrimers are particularly suited for membrane?ltration.20

Alternatively,the immobilisation of catalysts can be effected on inorganic matrices,having several important potential advantages such as:(a)the remarkable ease of handling and use,(b)reduced product contamination by having the catalyst fully bound to the solid support,(c) relatively safe handling owing to full chemisorption of the possible toxic chemicals,(d)reduced environmental impact upon work-up,(e)good thermal and chemical stabilities,(f) good dispersion of the active catalytic sites,with a signi?cant improvement in the reactivity and(g)improve-ment in the reaction selectivity,due to the constraints of the pores and the characteristics of surface adsorption.21In general,they offer superior chemical,mechanical and thermal stability compared with the use of organic polymeric supports.

1.3.Solvents

Since most of the chemical reactions are performed in the solution phase,the solvent plays a crucial role to implement any transformation,either on a laboratory or industrial scale.22For a given process,the solvent will always condition the work-up,recycling and disposal techniques employed for the appropriate treatment of the reaction mixture and every one of its components.Within the context of green and sustainable chemistry,the endeavour to replace volatile organic solvents in organometallic catalysis for alternative more practical and environmentally friendly solvents must be highlighted.23Interesting approaches include catalysis based on aqueous systems,ionic liquids, supercritical media,or?uorinated phases. Nonetheless,it is known that many reactions proceed ef?ciently in the solid state.In fact,in some cases,solid-state organic reactions occur more ef?ciently and selectively than their solution counterparts,since molecules in a crystal are arranged tightly and regularly.In addition,the solvent-free reactions make syntheses simpler for process and handling,saving energy and preventing solvent waste, hazards and toxicity.24

1.3.1.Supercritical?uids(SCFs).Supercritical?uids are well established as useful solvents for extraction,chroma-tography and a few specialised reactions.25In spite of the fact that they have been used for large-scale industrial production for most of the20th century,only during the last decade have their special properties made them attractive solvents for modern synthetic chemistry.25d,26The proper-ties of SCFs are different from those of ordinary liquids and gases and are tunable simply by changing the pressure and temperature.They form a single-phase mixture with gaseous reactants,sometimes avoiding a rate-limiting mass-transfer step and therefore,enhance the reaction rates. scCO2is readily accessible,with a T c of318C and a P c of 73atm and is abundant,inexpensive,non-?ammable,non-toxic and environmentally benign.Non-polar organic solvents have a high solubility in scCO2and the solubility of polar,ionic,or polymeric compounds can be increased by the addition of a polar additive or an appropriate surfactant. In addition,scCO2facilitates the separation of reactants, catalysts and products,being a substitute for environ-mentally less acceptable solvents.27

Water near its critical point(T c3748C and P c218atm)also offers environmental advantages and possesses properties very different from those of ambient liquid water.The dielectric constant is much lower and the formation of hydrogen bonds is less favoured.As a result,high temperature water behaves like many organic solvents in allowing a high solubility of organic compounds in near-critical water and complete miscibility in supercritical water.28

1.3.

2.Ionic liquids(ILs).Ionic liquids can be generally de?ned as liquid electrolytes composed entirely of ions.By applying the melting point criterion,they can be considered as salts with a melting point below the boiling point of water.They are,however,better described as liquid compounds that display ionic-covalent structures.Most ILs have an organic cation and an inorganic polyatomic anion.The most commonly used cations in room temperature ionic liquids are alkylammonium,alkylphos-phonium,29N,N0-dialkylimidazolium and N-alkylpyri-dinium cations and the most commonly utilised alkyl chains are methyl,ethyl,butyl,hexyl,octyl and decyl. Although the pyridinium-and imidazolium-based chloro-aluminate ionic liquids share the disadvantage of being reactive with water,the more recent tetra?uoroborate, hexa?uorophosphate,nitrate,sulfate and acetate salts are stable towards hydrolysis.Their physical and chemical properties can be?nely tuned for a range of applications by varying the cations or anions.30

This fascinating group of chemicals exhibits a great potential to improve development in organic chemistry, due to their particular properties:a very wide liquid range, relatively wide electrochemically stable window,good electrical conductivity,high ionic mobility with strong ion–ion interactions,negligible vapour pressure,non-?ammability,excellent chemical and thermal stability and ability to act as catalysts.Reactions in ILs have different thermodynamic and kinetic behaviour,which often lead to improved process performance.Moreover,ILs allow an enhanced stability of organometallic reagents and bio-catalysts and an easy recovery,as well as possible recycling of homogeneous catalysts.

The potential for recyclability,ability to dissolve a variety of materials and the non-volatile nature of the ILs are some of their unique attributes responsible for their popularity. Although originally studied in electrochemistry,ILs are currently being explored as environmentally benign solvent substitutes in a variety of applications such as chemical synthesis,liquid–liquid separations,extractions,dissolution processes,catalysis,biocatalysis and polymerisation.31 More recently,they have also found application in asymmetric synthesis,32as well as in the synthesis of nanoparticles and other inorganic nanostructures.33

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It has recently been shown that there is a possibility of performing chemical reactions in ILs in conjunction with microwave irradiation,34as well as with separation routes utilising binary ionic liquid–scCO2systems.35

In spite of the fact that ILs are generally considered as environmentally friendly substitutes for volatile organic solvents,the environmental fate and any potential toxicity issues for most ionic liquids are not known,particularly with respect to alkylimidazolium systems.36In fact,so far,only a few toxicological and ecotoxicological data are available for this group of chemicals.More information seems to be needed in order to assess ILs with regard to sustainability and the principles of green chemistry.37On the other hand, although ILs are easy to obtain,their conventional preparation involves an excess of solvents and alkyl halides and,therefore, new efforts have emerged in a direction to minimize,at least,the amount of solvents in the reaction medium.38 1.3.3.Fluorous media.Fluorous chemistry can be considered as a complementary type of liquid-phase synthetic and separation methodology involving the use of ?uorine-containing reagents and solvents.39Fluorous solvents offer a unique perspective on a chemical reaction that allows one or more stages to be carried out without the need for volatile or noxious organic solvents,making the process simpler and more energy ef?cient and reducing the separation steps.Per?uoroalkanes,per?uorodialkyl ethers and per?uorotrialkylamines are the most common ?uorous solvents used,which are practically non-toxic. These solvents can be used in conjunction with a?uorous reaction component(reagent,catalyst,pre-catalyst,ligand, product,scavenger,protecting group,etc.),to which a ?uorous tag has been deliberately attached in order to make it soluble in?uorous solvents.It must be taken into account that the attachment of?uorous ponytails can signi?cantly change the reactivity of the?uorous reaction component, the insertion of two or three methylene groups before the ?uorous ponytail being necessary,in many cases,to decrease their strong electron-withdrawing effects.

The foundation of this methodology resides in the fact that the?uorous solvent has a low miscibility with common organic solvents.At a certain increased temperature,it is miscible with organic solvents but,when cooled,it splits into a biphasic system.A?uorous biphasic system can therefore,consist of a?uorous phase containing a?uorous-soluble reaction component and a second product phase, which may be any organic or non-organic solvent with limited solubility in the?uorous phase.40The?uorous biphasic reaction at the operating temperature can proceed either in the?uorous phase or at the interface of the two phases,depending on the solubilities of the reactants in the ?uorous phase.When the reaction is complete,simply cooling the system makes the?uorous solvent immiscible in the organic phase.The?uorous biphasic system therefore, combines the advantages of a one-phase reaction with biphasic product separation.

The?uorous biphasic concept has been successfully applied in stoichiometric chemical reactions utilising organic, inorganic,or organometallic?uorous-soluble reagents. Because of the nature of the?uorous media,the application of?uorous reagents is limited to apolar substrates,since the reactions of polar substrates may be too slow for practical applications.This concept has also found application in catalysis(where only transition-metal complexes have been converted into?uorous soluble entities through ligand modi?cation),in multistep organic synthesis and in combinatorial chemistry.41

The?uorous phase,together with ionic liquid approaches and supercritical?uid systems,offers a whole new repertoire of solvents that overcome many of the problems of volatile organics.

1.3.4.Aqueous solvents.In the most recent decades,the use of water as a reaction solvent or co-solvent has received much attention in synthetic organic chemistry,with some-times surprising and unforeseen results.42Despite the different advantages that the previous mentioned solvents can offer,water can still be considered as a unique solvent. Moreover,water is the‘solvent of Nature’and,therefore,its use in common chemistry can be regarded as biomimetic and biocompatible.There are many potential reasons to replace the classical organic solvents by water,such as cost, safety and environmental concern.In fact,aqueous procedures are often referred to as green,environmentally friendly,or benign.In addition,the unique solvation properties of water have been shown to have bene?cial effects on many types of organic reactions in terms of both the rate and selectivity.Furthermore,experimental pro-cedures may be simpli?ed,since isolation of organic products and recycling of water-soluble catalysts and other reagents can be achieved by simple phase separation. The main obstacle to the use of water as reaction solvent is the negligible solubility of the majority of organic compounds in water.This problem can be addressed by using aqueous organic solvents or phase-transfer agents.As will be shown in this review,aqueous-phase transition-metal catalysis,including asymmetric catalysis,has emerged as an important tool in the formation of carbon–carbon bonds.43

1.4.Reaction conditions

While some reactions occur spontaneously,most of them require activation.For carbon–carbon coupling reactions, chemical activation modes(i.e.,catalysis)are indispensable in order to make processes effective and selective.The association of several activation modes,however,emerges as a powerful synthetic strategy when the respective kinetic effects are convergent.Besides the classical thermal activation mode,new methods have emerged in the recent years,such as physical or physicochemical activation techniques,among others.Thus,microwaves and ultrasonic and high-pressure techniques have been added to the chemist’s repertoire as physical methods for accelerating chemical reactions.On the other hand,physicochemical activation results from interactions between the medium and the reactive molecules and can arise from the solvent or from added complexing molecules.Physicochemical activation can be applied through the action of solvophobic effects(microemulsions and vesicles),host–guest chemistry,etc.

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1.4.1.Physical activation.

1.4.1.1.Microwave.Microwaves are a form of electro-magnetic radiation.When molecules with a permanent dipole are placed in an electric?eld,they become aligned with that?eld.If the electric?eld oscillates,then the orientations of the molecules will also change in response to each oscillation.Most microwave ovens operate at

2.45GHz,wavelength at which oscillations occur4.9! 109times per second.Molecules subjected to this microwave radiation are extremely agitated as they align and realign themselves with the oscillating?eld,creating an intense internal heat that can escalate as quickly as108C per second.Non-polar molecules such as toluene,carbon tetrachloride,diethyl ether and benzene are microwave inactive,while polar molecules such as DMF,acetonitrile, dichloromethane,ethanol and water are microwave active. This technique proves to be excellent in cases where traditional heating has a low ef?ciency because of poor heat transmission and,hence,local overheating is a major inconvenience.44

Microwave-assisted synthesis is a relatively young science of increasing research interest,as evidenced by the number of papers and reviews appearing in the literature.45The most important advantage of microwave-enhanced chemistry is the reduction in the reaction times.Reactions that require hours or days of conventional heating may often be accomplished in minutes under microwave heating.More-over,reactions are not only faster,but proceed with higher purity and,consequently,higher yields.The dramatic acceleration and increased purity and yields of micro-wave-assisted reactions make them attractive to the increased demands in industry and,in particular,for combinatorial drug discovery.46In addition to being energy ef?cient,the possibility of employing milder and less toxic reagents and solvents,or even solvent-free systems,offers a further advantage of this heating technology.

1.4.1.

2.Ultrasound.Ultrasound generally designates acoustic waves with frequencies in the range of20–100MHz.This energy is insuf?cient to cause chemical reactions,but when ultrasound travels through media a series of compressions and rarefactions are created,the rarefaction of liquids leading to cavities.During rarefaction, the negative pressure developed by power ultrasound is enough to overcome the intermolecular forces binding the ?uid and tear it,producing cavitation bubbles.The succeeding compression cycle can cause the microbubbles to collapse almost instantaneously with the release of large amounts of energy.The enormous rise in local temperatures and pressures produces a dramatic bene?cial effect of reaction acceleration,with relatively short times being required for completing the reaction such that the decomposition of thermally labile products is minimised.47 The frequency of ultrasound has surprisingly little in?uence on the reactions within the range in which cavitation occurs. Of signi?cance is the fact that ultrasound affects both homogeneous and heterogeneous reactions.

1.4.1.3.High pressure.Pressure represents a mild non-destructive activation mode,generally respecting the molecular structure by limiting decomposition or further evolution of the products.Therefore,the speci?c effects of high pressure can be of important value for organic synthesis.48The kinetic pressure effect is primarily determined by the variation of volume due to changes in the nuclear positions of the reactants during the formation of the transition state.Related to volume requirements are steric effects since the bulkiness of the molecules involved in the transition state conditions the magnitude of the steric interactions.As a consequence,pressure affects volume changes and should have an effect on steric congestion. As a mild activation mode,pressure may be considered of value in the synthesis of thermally fragile molecules, permitting a lowering of the temperature.In addition,the selectivity is generally preserved or even improved under such conditions.

On the other hand,pressure can be combined with solvophobic effects.The effect of pressure on organic reactions in aqueous solutions is complex.The activation volume relative to hydrophobic effects is positive(meaning deceleration by pressure),whereas the activation volume due to hydrogen bonding is negative.In addition, electrostatic effects may also be involved in many reactions (negative activation mode).Nevertheless,the combination of pressure and solvophobic activation may be an interesting method to increase the reactivity of reluctant polar molecules.

1.4.

2.Physicochemical activation.

1.4.

2.1.Micellar solutions.Micelles are dynamic colloidal aggregates formed by amphiphilic surfactant molecules.These molecules can be ionic,zwitterionic,or non-ionic,depending on the nature of their head groups, their micelles being classi?ed in the same way.In dilute solutions,amphiphile molecules exist as individual species in the media and these solutions have completely ideal physical and chemical properties.As the amphiphile concentration increases,aggregation of monomers into micelles occurs and,as a consequence,these properties deviate gradually from ideality.This concentration is called the critical micellisation concentration.

During the formation of micelles,head group repulsions are balanced by hydrophobic attractions and for ionic micelles, also by attractions between head groups and counterions. Hydrogen bonds can be also formed between adjacent head groups.

It is well known that the rates and pathways of all kinds of chemical reactions can be altered by performing the reactions in micellar media instead of pure bulk solvents.49 Micelles are able to(a)concentrate the reactants within their small volumes,(b)stabilise substrates,intermediates or products and(c)orientate substrates so that ionisation potentials and oxidation–reduction properties,dissociation constants,physical properties,quantum ef?ciencies and reactivities are changed.Thus,they can alter the reaction rate,mechanism and the regio-and stereochemistry.For many reactions,rate increments of5–100-fold over the reactions in homogeneous solutions have been reported.In some cases,rate increments may be much higher and increments in the order of106-fold have been observed.

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1.4.

2.2.Microemulsions.When water is mixed with an organic liquid immiscible with water and an amphiphile, generally a turbid milky emulsion is obtained which,after some time,separates again into an aqueous and an organic phase.On the water-rich side,the mixtures consist of stable dispersions of oil droplets in water,which coagulate with rising temperature.A spongelike structure is obtained if the mixtures contain approximately equal amounts of water and oil.On the oil-rich side,dispersed water droplets are found, which coagulate with decreasing temperature.The size of the domains is a function of the amphiphile concentration and the volume fractions of water and oil.50

Since microemulsions contain both a polar component (water)and a non-polar component(oil),they are capable of solubilising a wide spectrum of substrates.The mechanism of solubilisation is similar to that in micellar solutions.The micelles are replaced by the oil domains,which are capable of solubilising all kinds of hydrophobic substances.The solubilisation of polar substances takes place analogously through the aqueous domains of the microemulsion.The solubilisation capacity of microemulsions is generally superior to that of the micellar solutions and can therefore, affect the rate and course of a certain reaction.

1.4.3.Electrochemical activation.Electrochemistry represents a convenient synthetic method in which electrons constitute clean and energetically ef?cient reactants.The development of the potentialstat turned electrochemistry into a common tool for organic synthesis.51In spite of the procedural simplicity,absence of side products derived from reagents and high ability for accomplishing selective oxidoreductions under very mild conditions,electro-synthesis still appears to be undervalued,even though some industrial-scale work has demonstrated its appealing features.

The apparatus required for electrosynthesis can be as simple as a beaker containing a pair of electrodes connected to a direct-current voltage source.A stirrer,thermometer,jacket, inert gas inlet,or any combination,can be added.For some reactions,the separation of the electrodes by a diaphragm is mandatory to prevent the products from one electrode diffusing to the other and being destroyed.A proper solvent and supporting electrolyte will be also required.

In some cases,chemical techniques turn out to be quite dif?cult in the preparation of certain organometallic species. Electrochemistry can,however,provide an easy way to generate a desired oxidation state of a metal complex that becomes the active catalytic species for an organic reaction. In the particular case of redox processes,the active catalytic species can be recycled continually by the electrode oxidation or reduction reactions.In these processes,the electrons are consumed stoichiometrically with respect to the substrate.Therefore,it is the electrons that are used as clean,controlled and non-polluting redox agents.In non-redox reactions,electrochemistry is used only to generate the catalytic system.It has been observed that electro-generated species can be more reactive than their chemically prepared analogues.521.5.Miscellaneous non-conventional techniques

The techniques mentioned below are rather speci?c and so far have only been described for a limited number of examples.

1.5.1.Nano?ltration.It is important to recognise that the total ef?ciency of synthesis is also conditioned by the ability to separate the products from the unchanged starting materials,excess reagents and catalysts.Within the green chemistry context,it is also interesting to develop techniques that enable the separation and re-use of catalysts and reagents.Thus,separation protocols additional to those described above(i.e.,per?uorinated systems,sc?uids,ionic liquids,solid-phase supported reagents and catalysts,etc.), which are easily automated to enable rapid puri?cation by simple operations,are welcome.53

In the?eld of homogeneous catalysis,separation of the catalyst from the product mixture is rather complicated, preventing large-scale industrial processes.An interesting and promising development in the area of homogeneous catalyst recycling is the attachment of homogeneous catalysts to soluble organic supports.In this way, macromolecular catalysts anchored on soluble supports such as polymers and dendrimers are created,which can be recovered by ultra-or nano?ltration techniques and re-used again.

Recently,solvent-stable ultra-and nano?ltration mem-branes have been introduced showing high retentions for medium-sized soluble molecules.54In the?eld of mem-brane?ltration,ultra-and nano?ltration techniques are de?ned to retain macromolecules with dimensions between 8–800and0.5–8nm,respectively.

1.5.

2.Microreactors.Microreactor devices consist of a network of micron-sized channels(10–300m m),with a high surface-area-to-volume,etched into a solid substrate.55For solution-based chemistry,the channel networks are con-nected to a series of reservoirs containing chemical reagents and products to form the complete device with overall dimensions of a few cm.Reagents can be brought together in a speci?c sequence,mixed and allowed to react for a speci?ed time in a controlled region of the channel network using electrokinetic(electro-osmotic and electrophoretic)or hydrodynamic pumping.For electrokinetically driven systems,electrodes are placed in the appropriate reservoirs to which speci?c voltage sequences can be delivered under automated computer control.This control offers an effective method of moving and separating reagents within a microreactor,without the need for moving parts.Hydro-dynamic pumping uses conventional,or microscale,pumps to manoeuvre solutions around the channel network,but, this technique has the disadvantage of requiring either large external pumps or complex fabrication of small moving parts.

Many reactions have been demonstrated to show altered reactivity,product yield and selectivity when performed in microreactors,as compared with conventional benchtop glassware.In fact,the desired product is often produced in higher yield and purity and more quickly.Process

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parameters such as pressure,temperature,residence time and?ow rate are more easily controlled,thus minimising risk and side reactions.Furthermore,solvent-free mixing, in situ reagent generation and integrated separation techniques can all help to make the chemistry greener.56 One of the immediate applications is therefore in drug and process discovery,where the generation of compounds with different reagents under variable conditions is an essential factor and also allows,in a short time and with greater safety,a process to be transferred to the pilot and production scale.57

1.5.3.Ball-milling conditions.Ball-mill chemistry is of interest because of the mild conditions under which it operates and also the absence of any solvent and easy work up.This technique has,however,been scarcely studied and applied to very few reactions.58Apparently,the rotation of the steel balls creates a high pressure in contact with the walls of the container,allowing the reagents to interact and promoting the process.

2.Objectives and organisation

In principle,we wanted to present in this report the application of recent non-conventional methodologies to the transition metal-catalysed carbon–carbon coupling reaction.Heck,Suzuki,Sonogashira,Stille,Negishi and Kumada reactions,among others,were the reactions originally to be covered.Because of the abundant literature found on this topic,however,we decided to dedicate this ?rst part only to the Heck reaction,whereas the rest of the reactions will be studied in the second part in due course.

Nonetheless,the above introduction is common for any of the parts of the review.Other carbon–carbon bond forming reactions such as the transition-metal catalysed coupling reactions through the activation of carbon–hydrogen bonds, nucleophilic substitution(Tsuji–Trost reaction),or acyla-tion of carbon nucleophiles are beyond the scope of this review.Some of the reports dealing with the diverse topics to be tackled here have been previously and properly reviewed elsewhere and will not be covered to their full extent.Instead,a summary together with the more recent contributions until2004will be provided.The review is organised according to the sub-headings presented in the general introduction,taking into account the different components and variety of conditions involved in the Heck reaction.Many of the contributions to this review are also analysed from a critical point of view,with the aim of discussing the advantages and disadvantages that the different techniques offer and trying to select the best choice,when possible.A short conclusion can be found at the end of each section.

3.Introduction to the Heck reaction

The Heck reaction is broadly de?ned as Pd(0)-mediated coupling of an aryl or vinyl halide or sulfonate with an alkene under basic conditions.Since its discovery,this methodology has been found to be very versatile and applicable to a wide range of aryl species and a diverse range of ole?ns(Scheme2).59The major steps of the general and traditional mechanism for the Heck reaction are depicted in Scheme3.60

4.Substrates

4.1.Alternative arylating agents

In all the Heck reactions described in Scheme2,a stoichiometric amount of base is required to neutralise the acid that is formed during the reaction(see Scheme3).As a consequence,the corresponding equivalent amount of halide salt is obtained as waste.In the search for a cheap aryl source that does not lead to the formation of halide salts,de Vries et al.introduced the use of aromatic carboxylic anhydrides as the arylation source.61For instance,heating benzoic anhydride and n-butyl acrylate in a N-methylpyrrolidinone(NMP)solution containing PdCl2and NaBr at1608C for90min,led to the formation of(E)-n-butyl cinnamate with high conversion,90% selectivity and good yield.Although a catalytic amount of a chloride or bromide was necessary for optimal activity, phosphane ligands were not required.p-Methoxybenzoic anhydride and2-furanoic acid anhydride were also successfully used as arylation agents.A variety of ole?ns were arylated under similar conditions at140–1908C (Scheme4).Ole?ns with electron-withdrawing groups gave better yields,although,due to the relatively high reaction temperature,double-bond isomerisations and

less Scheme

2.

Scheme3.

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regioselective arylations were observed in some cases.It is noteworthy that the only side products in the reaction are benzoic acid(easily recovered by extraction with hot water) and carbon monoxide(which could be transformed into carbon dioxide in industrial processes).

Further investigation on this topic by Shmidt and Smirnov showed that the use of lithium chloride instead of sodium bromide increased the catalyst activity and productivity, since chloride accelerates CO elimination from the oxidative addition product more than bromide.62

Goo b en et al.studied the decarbonylative ole?nation of aryl esters in an attempt to minimise the production of waste.63 Starting from the p-nitrophenyl ester of the carboxylic acid, the corresponding alcohol formed in the Heck reaction could be recycled back into the starting ester,with CO and water being the only by-products in the overall reaction.63a Lithium chloride and isoquinoline proved to increase the effectiveness and stability of the catalyst in such a manner that higher yields were obtained.A wide variety of benzoates of electron-de?cient phenols(e.g.,p-nitrophenol) were found to be suitable substrates,whereas both electron-rich and electron-poor ole?ns gave similar yields,with regioselectivities ranging from4:1to20:1(Scheme5).If we compare this methodology with that described above,the scope of this Heck ole?nation seems to be wider.The catalytic system,however,requires larger amounts of all of its components,as well as the presence of a substantial amount of isoquinoline that must be removed at the end of the process.The lower reactivity of the benzoic esters in comparison with the benzoic anhydrides is also re?ected in the reaction times.The above idea was extended recently to the use of isopropenyl arenecarboxylates as arylating agents in a salt-free medium.63b These arylating reagents were syn-thesised through a waste-free reaction involving ruthenium-catalysed addition of the carboxylic acids to propyne. Concerning the coupling reaction,instead of waste salts,CO and acetone are the only by-products,the volatility of which allows easy workup.Electron-rich and electron-de?cient aryl,heteroaryl and vinyl carboxylic acid esters were coupled with several ole?ns(styrene in most cases)in good to excellent yields(Scheme6).In contrast to the bene?cial features of the whole process,the reaction temperature is rather high and is probably the reason for the moderate regioselectivities generally obtained(5:1–15:1),except in the case of n-butyl acrylate(O50:1).

In the examples shown in Schemes4and5,there is the necessity to generate the starting material in an extra reaction step and separate the ole?n products from the carboxylic acids or phenols,these being practical dis-advantages for small-scale preparations.Goo b en et al. utilised mixed anhydrides of carbonic and aromatic carboxylic acids,easily prepared in situ by mixing the carboxylic acids with di-tert-butyl dicarbonate(Boc2O),as arylating agents in the Heck ole?nation.64Different aromatic and heteroaromatic carboxylic acids(including electron-rich carboxylic acids)were coupled mainly with styrene,to give the expected products in moderate to good yields(45–88%)and selectivities(5:1–28:1)(Scheme7). The reaction could be performed at a lower temperature (1208C),in comparison to the examples described above, although g-picoline was necessary to stabilise the

palladium Scheme

4.

Scheme

5.

Scheme

6.

Scheme7.

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and to avoid precipitation and loss of activity at reasonable reaction rates.

Myers et al.subjected a wide range of arenecarboxylates to ef?cient Heck-type decarboxylative coupling with ole?nic substrates under relatively mild reaction conditions and in short reaction times (Scheme 8).65The key additive,silver(I)carbonate,presumably functions both as a base and as a stoichiometric oxidant,enlarging the lifetime of the active catalyst.Good yields of the coupled products were obtained for both electron-rich and electron-withdrawing substituents on the aromatic carboxylic acid and ole?nic partners such as styrene,acrylates,(E )-ethyl crotonate and cyclohexenone.Certainly this methodology allows the direct use of aromatic carboxylic acids without any previous transformation,although the experiments suggested that at least one ortho substituent is necessary for successful decarboxylative palladation to occur.The relatively high catalyst loading and the large amount of the silver salt used are the main disadvantages of this methodology,which probably would limit its application to a laboratory scale.

In 1982,Blaser and Spencer demonstrated that aroyl chlorides could react with activated alkenes,under Pd(OAc)2catalysis in the presence of a tertiary amine at 120–1308C,to give the expected (E )-arylalkenes stereo-speci?cally and in high yields.66More recently,Miura et al.have utilised the rhodium complex [(C 2H 4)2RhCl]2for the catalytic decarbonylative Heck-type coupling of aroyl chlorides with styrene and n -butyl acrylate.67This methodology is very interesting,since the reactions are carried out in the absence of any phosphane ligand and base and with low catalyst loading,although re?uxing o -xylene (143–1458C)is needed to obtain the products with good yields at reasonable reaction times (Scheme 9).In addition,the workup seems to be signi?cantly simple,that is,?ltration,evaporation and washing with an appropriate

solvent such as methanol.A slow stream of nitrogen is,however,required to sweep away the HCl and CO evolved during the reaction,what can be a limitation for large-scale processes.Under similar conditions,cyclic alkenes such as norbornenes also reacted with aroyl chlorides accompanied by cyclisation to afford the indanone derivatives.

Andrus et al.have recently applied a palladium-catalysed decarbonylative Heck-type reaction of aroyl chlorides to the synthesis of resveratrol using palladium acetate,an imida-zolium carbene-type ligand and a non-coordinating amine base,N -ethylmorpholine.68The overall yield starting from the inexpensive resorcylic acid (53%)was higher compared to the aryldiazonium or mixed anhydride approach.Boronic acids have been used as arylating agents in Heck-type reactions by several groups.4b Uemura et al.showed,in 1994,that arylboronic acids reacted with alkenes in acetic acid at 258C in the presence of a catalytic amount of palladium(II)acetate,together with sodium acetate,to give the corresponding aryl-substituted alkenes in high yields.69Alkenylboronic acids also reacted with alkenes under similar conditions to give the corresponding conjugated dienes stereospeci?cally,but the product yields were lower compared with those from the arylboronic acids.A similar treatment of sodium tetraphenylborate (NaBPh 4)with alkenes afforded the corresponding phenylated alkenes in high yields,together with biphenyl and benzene as side products.Oxidative addition of a carbon–boron bond to Pd(0),formed in situ,to give an organopalladium(II)species was assumed to be the key step of these cross-coupling reactions.More recently,Lautens et al.utilised a rhodium complex to catalyse the coupling reaction of arylboronic acids and styrenes in an aqueous media (Scheme 10).70The best results were obtained with [Rh(COD)Cl]2and TPPDS as the water-soluble ligand.It was,however,necessary to add 0.5equiv of sodium dodecyl sulfate (SDS)as a phase-transfer agent to avoid hydrolytic deboronation when the

arylboronic acid had polar functional groups.Gene

?t et al.found out that,using m -TPPTC [tris(m -carboxyphenyl)-phosphane trilithium salt]as the water-soluble ligand instead of TPPDS,no SDS was necessary,due to the inherent surfactant effect of m -TPPTC.71This ligand exhibited a similar performance in comparison with TPPDS,but was shown to be superior to TPPTS under the same conditions depicted in Scheme 10,but in the absence of https://www.wendangku.net/doc/7e2513454.html,utens’methodology was very recently extended to the coupling of a wide variety of aryl-and hetero-arylboronic acids with acrylates,acrylamides and vinyl sulfones.72The high selectivities and yields obtained

were

Scheme

8.

Scheme

9.Scheme 10.

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believed to result from the use of the bulky,electron-rich, water-soluble ligand tert-butyl-amphos chloride[N-2-(di-tert-butylphosphino)ethyl-N,N,N-trimethylammonium chloride].

Different catalytic systems have been developed recently for the Heck-type reaction of boronic acids and electron-de?cient ole?ns(Scheme11).Pd(OAc)2,[Ru(p-cymene)Cl2]2and RhCl3were utilised as catalysts by Mori,73Brown,74Zou,75and their corresponding co-workers,respectively.Despite the palladium and rhodium catalytic systems exhibiting better yields,higher tempera-tures were also required in comparison with the ruthenium catalytic system.Stoichiometric amounts of Cu(OAc)2were needed as a re-oxidising agent for palladium and ruthenium, the latter including3-quinuclinidone as a base in order to obtain the highest turnover.

The groups of Jung and Larhed independently introduced molecular oxygen as a re-oxidising agent in the palladium(II)-catalysed coupling of organoboron compounds and ole?ns. The optimised catalytic system reported by Jung et al.was composed of10mol%Pd(OAc)2,O2and Na2CO3in DMF at508C for3–10h.76Under these conditions,electron-rich and electron-poor ole?ns could be coupled with several boronic acids and esters,with generally good yields and stereo-and regioselectivities.The catalyst loading was diminished to1mol%by Larhed et al.in a catalytic system composed of Pd(OAc)2,O2,N-methylmorpholine and 1.2mol%2,9-dimethyl-1,10-phenantholine in MeCN at 508C for3–24h.This oxidative Heck protocol was applied to the coupling of arylboronic acids with unsubstituted acrylates77a and electron-rich ole?ns.77b The internal regioselectivity observed for the coupling with n-butyl vinyl ether and enamides was attributed to the phenanthro-line ligand,which also seemed to mediate the re-oxidation of palladium(0)with molecular oxygen,allowing a low catalyst loading.

Together with boronic acids,arylsilanols78and arylstan-nanes78c,79have been used as arylating agents in the Heck reaction with electron-de?cient ole?ns.There are,however, some evident disadvantages of these materials,when compared with the carboxylic acid derivatives.Firstly, these starting materials are not so readily available,their preparation involving less common and more expensive reagents,with the corresponding generation of waste. Secondly,boric acid,silanols and stannanes are formed as by-products in the Heck reactions,which can make the puri?cation of the products dif?cult with a low possibility of recycling.Thirdly,the presence of large amounts of Cu(II) salts as re-oxidants,phosphanes and organic bases is required for a maximum ef?ciency.

Uemura et al.found that diphenyltellurium(IV)dichloride reacted with a variety of ole?ns in the presence of a catalytic amount of PdCl2,together with NaOAc in HOAc to afford the corresponding arylated(E)-ole?ns in variable yields (3–98%)(Scheme12).80A suitable oxidant such as tert-butyl hydroperoxide or copper(I)or copper(II)chloride had to be added for the reaction to proceed catalytically on palladium.The stereoselectivity was very high,except for acrylonitrile(Z/E26:74).Transmetallation of tellurium with palladium was suggested as the key step of the reaction. Alternatively,diaryltellurides could be used as arylating agents for a variety of ole?ns in the presence of Et3N as base and AgOAc as oxidant(40–99%product yield).81

As an alternative to the above reagents,Kamigata et https://www.wendangku.net/doc/7e2513454.html,ed aryldimethyltellurium iodides for the palladium-catalysed Heck-type reaction with electron-de?cient ole?ns and styrene,in the presence of a stoichiometric amount of silver(I)acetate.82For the telluronium salt partner,the best results were obtained when the aryl moiety bore electron-donating substituents at the para position,those at the ortho position retarding the reaction(Scheme13).The yields are good to excellent,although a3-fold excess(with respect to the ole?n)of the expensive silver acetate is needed for the anion exchange and oxidation steps in the catalytic cycle.In contrast with the reactions with organic tellurides,for which the crude mixtures must be puri?ed to remove the excess reagent,in the reactions with the telluronium salts the pure products were obtained by simple?ltration using silica gel to remove the solids in the reaction mixture. Unfortunately,the organic tellurides and tellurium salts are not commercially available.Diaryltellurium(IV)dihalides are normally prepared from TeCl4with activated arenes, arylmercury chlorides or arenediazonium

salts. Scheme

11.

Scheme

12.

Scheme13.

F.Alonso et al./Tetrahedron61(2005)11771–1183511781

Symmetrical diaryltellurides can be prepared from alkali tellurides and non-activated aryl halides,sodium telluride or potassium tellurocyanate and arenediazonium?uoro-borates,tellurium(IV)halides and arylmagnesium halides, or elemental tellurium and diarylmercury compounds.Alkyl aryl tellurides are the precursors of the corresponding telluronium salts and are generally prepared by sequential arylation–alkylation of sodium telluride or from organyl tellurolates,generated by tellurium insertion into organo-magnesium or organolithium reagents.83In short,the

preparation of these arylating agents represents a major disadvantage that adds to the toxic and mutagenic properties of the starting materials,tellurium and TeCl4,respectively, and to the possible toxicity of the organotellurium compounds.84

A variety of organoantimony compounds have also found application in the arylation of ole?ns with different catalytic systems,including:(a)triphenylstibine with AgOAc and catalytic Pd(OAc)2,85(b)diphenyl-and phenylantimony chloride with catalytic Pd(OAc)2under air,86(c)triaryl-antimony diacetates under PdCl2(MeCN)2catalysis87 and(d)triarylstibines88or tetraphenylantimony(V) carboxylates89in the presence of equimolecular amounts of a peroxide and catalytic amounts of Li2PdCl4or PdCl2 (see some selected examples in Scheme14).In spite of the fact that these antimony compounds cannot be considered as usual reagents,all of them have an interesting feature in common,namely that the coupling reactions can be carried out under very mild reaction conditions,normally at room temperature or508C.

Less common is the use of organolead(IV)compounds as arylating agents for ole?ns.Kang et al.described in1998for the?rst time that aryllead triacetates could be coupled with a variety of electronically different ole?ns under mild reaction conditions and palladium catalysis(see one example in Scheme15).90Most of the reactions proceeded at room temperature with moderate to good yields,although the homocoupling reaction competed in some of the experiments reported.It was presumed that the oxidative addition step was facilitated by the formation of the organolead trimethoxide,ArPb(OMe)3,to give a polar reactive intermediate,ArPdPb(OMe)3,which allowed the coupling under mild conditions.On the other hand,the aryllead triacetates are not commercially available and are rather toxic reagents.

Most of the alternative arylating agents presented in this report have the main advantage of minimising by-product formation,therefore facilitating the work-up.Except in the case of the carboxylic acids,however,the rest of the reagents are not commercially available and the generation of waste in their preparation is inevitable.In addition,rather high temperatures are needed for the coupling reactions in order to achieve reasonable conversions.

4.2.Supported substrates

Intermolecular Heck reactions on solid supports have been extensively used in synthetic organic and combinatorial chemistry,due to the easy accessibility of the starting halo-alkenes or-arenes and alkenes.The reactions involve immobilised aryl halides,mostly iodides,or iodonium salts with soluble alkenes,or immobilised alkenes with soluble aryl halides.When performed on the same type of resin and with the same catalytic system,the immobilisation of aryl iodides appears to be more bene?cial than that of alkenes. Two main protocols have been applied:(a)the standard Heck conditions[Pd(OAc)2,Ph3P or(o-Tol)3P,DMF,80–1008C],2–24h]and(b)the Jeffery conditions[Pd(OAc)2, Ph3P,TBAC,K2CO3,DMF,20–808C].The intramolecular Heck reaction on solid supports has found application in the preparation of macrocycles and heteroatom-containing ?ve-,six-and seven-membered rings,as well as in the construction of indoles,benzofurans,dihydroisoquinolines and benzazepines.The pseudo dilution effect exhibited by the starting material in the intramolecular version has led to an increased yield.Both inter-and intramolecular Heck reactions on a solid support have been recently reviewed17 and,therefore,it is not our objective to repeat all of this information here.Instead,we will deal with the more recent and representative examples and present a general con-clusion at the end of this section.

Morphy et al.observed that the use of low solvent volumes in solid-phase Heck reactions resulted in large increases in yield,compared with the standard dilution conditions.91 3-Iodobenzoyl chloride was reacted with Wang resin,the resulting aryl halide being coupled with ethyl acrylate under palladium catalysis,followed by resin cleavage with

TFA. Scheme

14.

Scheme15.

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11782

After reaction at608C for2h at standard dilution(1ml),a conversion of40%was observed,compared to80%when only0.05ml of solvent was used.The reaction was complete after18h for a low solvent volume with only 54%conversion under standard dilution conditions (Scheme16).The optimal amount of solvent represented %2m L/mg of resin,signi?cantly less than that required to totally swell the resin used and lead to a separate solvent phase.This methodology is certainly advantageous,since it minimises the use of solvent and provides high conversions under mild reaction conditions.Unfortunately,all reactions were performed on a very small scale(0.05mmol of resin-bound3-iodobenzoic acid)with excess of ethyl acrylate (2equiv)and Et3N(5equiv)and,therefore,the behaviour of this catalytic system on a larger scale remains uncertain.

A small library of cinnamate esters was prepared by Gene?t et al.,based on the use of a new stable silylated polystyrene, PS-SiMe2CH2Cl.92This chloromethyl resin was esteri?ed with various iodobenzoic acids(o-,m-and p-derivatives),followed by a cross-coupling reaction with ethyl acrylate in DMF in the presence of Pd(OAc)2-PPh3as the catalytic system,the latter transformation taking place with complete conversion.The expected esters were released from the resin by treatment with TBAF in THF(Scheme17).Owing to the dif?culties of eliminating the excess of TBAF, however,further treatment with Amberlyst A-15and its calcium salt as scavengers was needed to purify the reaction mixture.Despite the?nal products being obtained in good yields and the mild resin-cleavage step,this methodology does not seem to introduce any advantage with respect to the use of the more conventional resins.Firstly,the silylated resin is not commercially available and had to be prepared from a1%divinylbenzene–styrene copolymer by lithiation and trapping with chloro(chloromethyl)dimethylsilane,a relatively expensive electrophile.Secondly,the cesium carboxylate had also to be prepared to increase its nucleophilicity in the S N2reaction to attach the resin. Thirdly,a special resin-cleavage protocol was needed, leading to more waste(additional to the excess of reagents) and to the generation of a new silylated resin with no chance of being recycled.

Takahashi et al.recently described the stereoselective synthesis of36peptides containing unnatural amino acids, utilising the Pd(0)-catalysed Mirozoki–Heck reaction of dehydroalanine derivatives in combination with an asym-metric hydrogenation on polymer support.93In this case, the alkene partner was supported on Synphase Rink-amino PS-Crowns e,whereas the aryl iodides were in solution.It was found that4mM Pd(dba)2in MeCN at808C for3h in the presence of TBAC and Et3N were the optimal reaction conditions.Products were obtained with a high purity, except for aryl iodides bearing electron-withdrawing substituents,where a low purity(45–60%,p-AcC6H4I)or no reaction(p-NO2C6H4I)was observed(Scheme18). Asymmetric hydrogenation and?nal cleavage with TFA–CH2Cl2furnished the corresponding

phenylalanine Scheme

16.

Scheme

17.

Scheme18.

F.Alonso et al./Tetrahedron61(2005)11771–1183511783

derivatives with high stereocontrol.Unfortunately,the authors did not give any information about the isolated yields of the ?nal products,making it dif?cult to evaluate the ef?ciency of the whole process.

Portnoy et al.synthesised various poly(aryl benzyl ether)dendrimers on a solid support,based on the initial immobilisation of commercially available 5-hydroxy-isophthalate onto the Wang resin,followed by ester reduction.Repetitive Mitsunobu coupling and ester reduction led to the formation of a second and third-generation of dendrimers.94The three resins were subjected to Mitsunobu reaction with p -iodophenol,followed by Heck coupling with methyl acrylate,with complete conversions being achieved for every resin.Only moderate yields and fair purities were,however,obtained for any of the resins tested upon TFA-induced cleavage (Scheme 19).In fact,this methodology has no advantage with respect to that developed by Hanessian et al.95in which the aryl iodide was directly attached to the Wang resin.In this case,the free cinnamic ester was obtained in 90%overall yield under the same reaction conditions,but minimising the number of steps and consequently,the generation of waste,making the process more economic and time saving.

In a study on indole synthesis,Kondo et al.described the palladium-catalysed intramolecular cyclisation of enamino-esters in the solution phase and on solid supports.96In the solution phase,the expected ethyl 3-phenyl-2-indole-carboxylate was obtained in 56%yield after treatment with a catalytic amount of Pd 2(dba)3,(o -Tol)3P and Et 3N in DMF at 1208C for 2h (Scheme 20).The polymer-supported version of this reaction involved the attachment of the substrate to a hydroxymethyl-polystyrene resin,treatment with the same catalytic system at 1108C for 12h,and ?nal transesteri?cation of the resulting polymer-bound indole carboxylate using NaOMe in MeOH–THF.In this case,the product was obtained in 48%yield after further puri?cation by column chromatography.It seems clear that the solution-phase reaction is advantageous,since it reduces the reaction time in the intramolecular coupling,less steps are used,and the yield is slightly improved.Similar solid-phase indole synthetic strategies have been published recently by the same research group.97

It is clear that the main reason for immobilising a molecule on a solid support for the Heck or any other reaction relies on the simple separation of the intermediates and,?nally,of the products from the reagents and soluble by-products.This fact,which represents a major advantage,compared to the solution-phase chemistry,may hide some inherent incon-veniences and limitations that can curtail the whole ef?ciency of the process,for example,(a)reactions can be driven to completion in most cases,but only in return for consuming an excess of reagent,(b)suitable,robust and versatile linkers are required,which have to be cleaved selectively under mild reaction conditions without destroy-ing the product,(c)a second functionality in the starting material is normally necessary for attachment to the support,as exempli?ed by the intermolecular Heck reaction,in which the polymer-bound aryl iodides must bear an additional group (carboxy,hydroxy,amino,etc.)that remains at the end in the product,whereas most of the polymer-bound alkenes studied are derived from a ,b -unsaturated carboxylic acid derivatives,(d)the selection of usable solvents and the temperature range can be quite restricted (1008C is at the upper limit),(e)the chemistry involving heterogeneous catalysts such as palladium on charcoal is incompatible with solid-phase synthesis methods,(f)the dif?culty of analysing the outcome of a given reaction makes it necessary for the cleavage of the products from the support to be analysed by normal methods and (g)in the case of solid-phase combinatorial chemistry,additional investment is essential for laboratory automation,robotics and mechanical and tag-reading/sorting devices enabling the simultaneous performance of multiple tasks.In short,there is a need for more solid-phase methodology,including the development of traceless

linkers.

Scheme

19.

Scheme 20.

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5.Catalytic systems

The selection of a proper catalytic system is fundamental for achieving the best ef?ciency in a given Heck reaction.In order to design such an ef?cient catalytic system,however, we have to focus not only on its catalytic activity or selectivity,but also on other important topical issues,such as the possibility of recovery of the components,or their toxicity and environmental impact,especially for appli-cation to an industrial scale.In fact,industrial applications

are rare,because the cheap aryl chlorides or many readily available bromides do not react with suf?ciently high yields, turnover numbers and selectivities,even in the presence of the traditional phosphane catalysts.98Signi?cant efforts have been made in recent years to develop more ef?cient catalytic systems,trying to simplify these reactions as much as possible.

5.1.Ligands:ligand-free catalytic systems

Tertiary phosphane ligands have traditionally been used to ensure catalyst stability,in spite of the fact that they can have some detrimental effect on the rate of the individual steps of the coupling reaction.The use of phosphorus ligands in?ne-chemical and industrial processes,however, is less desirable.They are usually toxic,unrecoverable and frequently hamper the isolation and puri?cation of the desired product,as well as the performance of consecutive catalytic steps of the total synthesis.In spite of the fact that numerous phosphane-free ligand systems have been developed,including palladacycles,nucleophilic carbene ligands and others,99these catalytic systems suffer from some drawbacks.The high ligand sensitivity to air and moisture,their tedious multistep synthesis,the high cost of the ligands and the use of various additives curtails their applications.On the other hand,the ligand-free Heck catalytic systems have very recently emerged as more advantageous at all levels,operationally,economically and environmentally.100

We have described in Section4.1a series of methodologies involving the use of alternative arylating agents to aryl halides in the Heck reaction,most of which have a common and advantageous feature,that is,no ligand was added to the reaction mixture.The ligandless approach to carbon–carbon coupling was,however,pioneered independently by Beletskaya101and Jeffery.102The latter author reported,in 1984,the palladium-catalysed vinylation of organic iodides under solid–liquid phase-transfer conditions at,or near, room temperature,using TBAC as the phase-transfer agent and sodium hydrogen carbonate as a base in the absence of any ligand.102a The reactions proceeded with excellent yields(85–98%)and with high regio-and stereoselectivity. Aryl iodides furnished the(E)-products exclusively (Scheme21),whereas(E)-1-iodohexen-1-ene gave a1:15 diastereomeric mixture in favour of the(E,E)-product.The mild conditions allowed this type of reaction to be generalised to thermally unstable vinylic substrates such as methyl vinyl ketone or acrolein.Fortunately,the vinylation of vinylic iodides was greatly accelerated (1–5h)by using potassium carbonate instead of sodium hydrogen carbonate as the inorganic base,with a parallel improvement of the stereoselectivity.102b More recently,a slightly modi?ed catalytic system was applied by Crisp et al.to the Heck coupling of the chiral non-activated alkenes,2-aminobut-3-en-1-ols,with cyclo-hexenyl tri?ate.103In this case,tetra-n-butylammonium tri?ate was used instead of TBAC under mild reaction conditions,the produced dienes being isolated in moderate to good yields and with little or no racemisation (Scheme22).The high reactivity observed with tetra-n-butylammonium tri?ate was attributed to the high rate of dissociation of the tri?ate anion from the neutral palladium(II) intermediate and the formation of a very reactive cationic palladium species.Some bene?cial in?uence was observed when a small amount of water(5equiv)was added to the reaction mixture.Little can be said about the scope of this reaction,since cyclohexenyl tri?ate was the only tri?ate tested.

A very simple catalytic system was used by Gundersen et al. in the coupling of vinylpurine with a variety of aryl iodides (Scheme23).104Better results were obtained when Pd(OAc)2alone was employed as the catalyst compared with catalysts containing phosphane ligands such as triphenylphosphane.All the couplings were highly stereo-selective,including the coupling of vinylpurine with(E)-methyl

3-iodo-2-methylacrylate.

Scheme

21.

Scheme

22.

Scheme23.

F.Alonso et al./Tetrahedron61(2005)11771–1183511785

Buchwald et al.introduced the bulky amine base,methyl(dicyclohexyl)amine,into a phosphane-free catalytic system that found application in the coupling of aryl iodides and bromides with 1,1-and 1,2-disubstituted ole?ns to give trisubstituted ole?ns (Scheme 24).105The method was applicable to the coupling of both electron-de?cient and electron-rich substrates and displayed good stereoselectivity and a high degree of functional-group compatibility.A combination of the bulky amine and tetraethylammonium chloride (TEAC)made the reaction faster and increased the E /Z selectivity,in comparison with other amines.

Reetz et al.discovered that Pd(OAc)2in the presence of the additive,N ,N -dimethylglycine (DMG),is a simple,reactive and selective catalytic system for the Heck reaction of aryl bromides with ole?ns.106The reaction of bromobenzene and styrene in NMP took place with O 95%trans-selectivity with only traces of side products in the presence of a 20:1DMG/Pd ratio (Scheme 25).It had been interesting to know the isolated yields instead of the conversions,as well as the experimental procedure for the product puri?cation,above all taking into account the presence of the additive DMG and the high boiling point solvent NMP.

Another simple catalytic system recently developed by Schmidt et al.was found to catalyse the reaction of bromoarenes with styrene in air in the absence of any ligands.107Conversions of around 95%were achieved by the use of 0.04–1.6mol%PdCl 2,18%HCO 2Na and 112%NaOAc in DMF after 10min at 1408C or 180min at 1008C (Scheme 26).The presence of sodium formate as a reducing agent accelerated the reaction,although it had no effect on the yield of stilbene.It was corroborated that colloidal palladium particles formed in the course of the reaction are the main reservoir of catalytically active homogeneous Pd(0)complexes.The low catalyst loading,the availability and the low prices of the components of the catalytic system,together with the absence of an inert atmosphere,

makes this methodology attractive to be applied at a larger scale.The 6-fold excess of bromoarene required is,however,an important limitation,above all taking into account that bromoarenes are rather expensive and that an additional recycling strategy should be developed for better process ef?ciency.In our opinion,this work demands further study on the applicability to some other aryl bromides and alkenes,as well as a study on the compatibility of different functional groups attached to the substrates with the reaction conditions.

In this context,Pd(OAc)2in combination with K 3PO 4in DMA exhibited a high catalytic activity for the Heck reaction of both activated and deactivated aryl bromides in the absence of any stabilising ligands or additives.108Styrenes and vinylcyclohexene led to the expected coupling products with good to excellent isolated yields (63–98%)when the reaction was performed at 1408C for about 20h (Scheme 27).It is,however,surprising that the more activated terminal ole?ns such as n -butyl acrylate gave low yields.

The group of de Vries has recently concentrated much effort in developing ligand-free palladium catalytic systems for Heck reactions,for example,they reported a practical and cost-effective coupling methodology based on the recovery and re-use of the palladium catalyst,109with different Heck reaction mixtures being separated from precipitated palladium on Celite by ?ltration.The addition of 2equiv of iodine or bromine in NMP dissolved the recovered palladium and allowed the performance of eight successive runs without signi?cant loss of activity.This re-activated palladium catalyst,which is homogenous in character,was suggested to exist as a mononuclear anionic species,although the presence of nanoparticles was not excluded.The same research group proved that the catalytic system reported by Reetz et al.106(see Scheme 25)could work nicely in the absence of the additive DMG and with a lower catalyst loading.A broad range of aryl bromides was reacted with both electron-de?cient and electron-rich ole?ns in the presence of 0.05mol%Pd(OAc)2,and 2.4mmol of NaOAc in NMP at 1358C for 1–15h,affording the products in 80–100%conversion.110The fact that this method was scaled up to a few Kg,together with the low cost of the

catalytic

Scheme

24.

Scheme

25.

Scheme

26.

Scheme 27.

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system,the relatively low solvent volume used and the easy workup procedure,makes it very attractive for large-scale production.

As an example of a speci?c application,a ligand-free palladium-catalysed Heck reaction of methyl2-acetamido-acrylate and aryl bromides was used by de Vries et al.as the key step in the synthesis of enantiopure substituted phenylalanines.111All reactions were performed in NMP at1258C in the presence of Pd(OAc)2,BnNEt3Br and Pr2i NEt or NaOAc as base.A variety of aryl bromides with different electronic character was tested,giving rise to the corresponding products,puri?ed by simple crystallisation, in moderate yields(Scheme28).It is noteworthy that one of the reactions took place in55%yield,even in the absence of the tetraalkylammonium salt,simplifying the catalytic system even more.

The absence of any ligand in the reaction medium, especially phosphane ligands,is very desirable.This absence,however,normally implies the presence of other additives to stabilise the in situ generated palladium species, which nonetheless can be removed more easily.At any rate, more efforts are needed for the ligand-free Heck reaction in order to decrease the reaction temperature,above all in the coupling of aryl bromides.

5.2.Catalysts:supported catalysts

Although the Heck reaction is also very attractive also for industrial applications,the homogeneous Heck reaction has no practical application in industry.112The loss of catalyst, which usually cannot be recovered and the need for aryl bromides or iodides as the starting materials are the major drawbacks that have prevented a more extensive exploita-tion of this reaction at an industrial level.The loss of catalyst could perhaps be tolerated if the cheaper and much more readily available aryl chlorides could be employed as the starting materials.

In principle,heterogeneous catalysts or heterogenised homogeneous catalysts can be used to solve some of the above-mentioned technical applications in the Heck reaction.113Among the heterogeneous catalysts we should mention the supported metal catalysts,zeolite-encapsulated catalysts,colloid-nanoparticles and intercalated metal compounds.The homogeneous metal complexes catalysts can be heterogenised using modi?ed silica catalysts,polymer-supported catalysts,biphasic catalysts,supported liquid-phase catalysts,non-ionic liquid solvents,per?uori-nated solvents and re-usable homogeneous complexes.All these types of catalysts can be easily recovered from the reaction mixture and recycled,if they do not deactivate too quickly under duty.In addition,the palladium in hetero-geneous catalysts would already be present as metal crystallites dispersed onto the solid support,so that precipitation of palladium black should not occur.In general,the heterogeneous catalysts have a major drawback of lower selectivity towards Heck coupling and metal leaching,whereas the heterogenised metal complexes operate under milder reaction conditions.

Since an important part of this topic has been tackled in diverse reviews,we are going to deal mainly with some selected examples of the most recent literature covering the study of catalysts supported on carbon,metal oxides, molecular sieves,clays,zeolites,polymeric and dendrimeric materials,among others.

5.2.1.Carbon.Palladium on carbon proved to be active for Heck coupling under several different conditions and is one of the most frequently investigated catalysts.113In general, carbon-supported catalysts do not seem to differ signi?-cantly in activity from their homogeneous counterparts, since the proportion of the metal to the limiting reagent, reaction temperatures,times and yields are comparable to those observed for homogeneous catalysts.Palladium supported on carbon,however,often causes unwanted hydrodehalogenation of the haloaromatic compounds and suffers from substantial palladium leaching.114Palladium leaching is also relevant to the mechanism of Pd/ C-catalysed Heck couplings.In fact,it is still the subject of debate as to whether the reaction takes place on the solid palladium surface or the true catalyst is the dissolved palladium that has been leached from Pd/C,which acts simply as a palladium reservoir.

It is worth mentioning the publication by Beller et al.which described the?rst Heck reaction of aryldiazonium salts using heterogeneous catalysts.115Palladium on carbon was shown to be a very effective catalyst in this reaction under very mild conditions(40–608C)(Scheme29).There was no need to add stoichiometric amounts of base or stabilising ligands such as phosphanes and these are major advantages. Unfortunately,the catalyst exhibited an important reduction in activity after its?rst use.The lack of commercial availability of the starting anilines and the additional step of conversion into the corresponding aryldiazonium

salts Scheme

28.

Scheme29.

F.Alonso et al./Tetrahedron61(2005)11771–1183511787

would be the only possible disadvantages of this methodology.

A very interesting and detailed study was reported by Ko

¨hler et al.concerning the Heck reaction of aryl bromides with ole?ns in the presence of a variety of Pd/C catalysts.116The activity of the catalysts was shown to be strongly dependent upon the palladium dispersion,palladium oxidation state in the fresh catalyst,the water content and the conditions of catalyst preparation.A high palladium dispersion,low degree of palladium reduction,high water content and uniform palladium impregnation led to the most active catalyst.The fact that uniformly impregnated Pd/C catalysts showed higher activities than eggshell catalysts supported the hypothesis that leached palladium is the active species,for which the solid Pd/C acts as a reservoir that delivers catalytically active palladium species into solution.In fact,Arai et al.have demonstrated that palladium exists on the support,in solution and in the form of free colloidal particles during and after the Heck reaction,which can be redeposited on the support.117The optimised Pd/C catalyst exceeded by at least one order of magnitude the activity of any heterogeneous palladium catalyst reported in the literature in the reaction of bromoarenes with ole?ns (Scheme 30).In general,all the catalysts studied exhibited a high activity and selectivity,without the exclusion of air and moisture,extremely low palladium concentrations,easy and complete separation from the product mixture,easy and quantitative recovery of palladium and commercial availability.Although the TONs were still lower than those of the most active homogeneous catalytic systems for the activation of aryl bromides,the TOFs were higher,the activity at the beginning of the reaction being extremely high before deactivation of the catalyst occurred.In contrast to the results of Arai et al.,118who observed up to 80%hydrodehalogenation,no hydrodehalogenation of bromoarenes was observed in any experiment.

Hara et al.obtained quasi 2-dimensional palladium nanoparticles encapsulated into graphite,which proved to be active catalysts for the Heck reaction.119Thus,an 82%yield of the coupled product,stilbene,was isolated by reacting 1mmol of styrene with 2mmol of iodobenzene in the presence of 4mmol of potassium carbonate,2mmol of tetra-n -butylammonium bromide and 10.2mg of the quasi two-dimensional palladium particles encapsulated in graphite (37%)in DMF using a sealed tube at 1008C for 4days (Scheme 31).No coupling product was observed with chlorobenzene.The nanoparticles remained inside the

carbon lattice after the Heck reaction and could not be washed out,the catalyst therefore being stable.Despite this catalytic system completely avoiding palladium leaching,its preparation is rather time consuming and somewhat complex.In addition,harsh reaction conditions and long reaction times are required.

For the application of Pd/C in combination with ionic liquids,see Section 6.2.

5.2.2.Metal oxides and other inorganic materials.The catalytic activity and selectivity of palladium supported on various metal oxides in the Heck reaction have attracted the interest of many research groups,both the nature of the oxide support and the Pd dispersion playing a crucial role in the activity of the catalytic system.120On the other hand,there is a considerable interest in determining the heterogeneous or homogeneous nature of the mechanisms involved in these reactions.121

Silica,within the family of metal oxides,has been,by far,the most utilised support in the Heck reaction.122In one of the ?rst reports on this topic,Strauss et https://www.wendangku.net/doc/7e2513454.html,ed 0.18%palladium on porous glass tubing for Heck reactions conducted continuously or batchwise.123This support offered resistance to oxidative deterioration and could be re-used several times for repeating,or for different,reactions,but the regio-and stereoselectivity was lower than expected.In parallel with this work,Mirza et al.developed a supported liquid-phase catalytic system for the Heck reaction of iodobenzene and methyl acrylate in a batch reactor,based on a combination of sulfonated triphenyl-phosphine–palladium complexes (Na-TPPMS and PdCl 2)supported upon porous glass beads and solvated with ethylene glycol (Scheme 32).Under these conditions,the catalyst complex was held in solution,whilst the reactants and products were restricted to a nonmiscible solvent phase.124Leaching was eliminated to the limits of detection,but the activity of the supported liquid-phase catalyst decreased signi?cantly after recycling.With regard to the nature of the catalysis occurring within the system,evidence suggests that this is predominantly homogeneous via the formation of an organic-soluble catalyst complex.Alter-natively,potassium acetate was used by Arai et al.as an inorganic base instead of triethylamine in a very

similar

Scheme

30.

Scheme

31.

Scheme 32.

F.Alonso et al./Tetrahedron 61(2005)11771–11835

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catalytic system,125whilst tri-n -butylamine gave higher reaction rates than triethylamine.126

A supported palladium catalyst on glass beads,generated from a guanidinium phosphane and palladium acetate,showed a high activity and low leaching of catalyst in the Heck reaction of aryl iodides and alkenes (Scheme 33).127The low catalyst loading,as well as the high yields achieved and the low leaching maintained over four reaction cycles,are clear advantages of this catalytic system.The main inconvenience is the preparation of the ligand which involves four steps,that is,Grignard reaction of com-mercially available 2-(N ,N -bis-trimethylsilylamino)phenyl-magnesium chloride with phosphorus trichloride,nitrogen deprotection,hydrochloride formation and condensation with dimethyl cyanamide.

The same research group prepared a new catalyst by treatment of reverse-phase silica beads with Pd(OAc)2and Ph 3P in cyclohexane.128The reverse-phase bead catalyst formed was assumed to contain (Ph 3P)2Pd(OAc)2and was stable in air and easy to handle.This catalyst was applied to the Heck reaction between iodobenzoic acid and acrylic acid,the expected product being obtained in a high yield and with low palladium leaching (Scheme 34).Heteroaromatic halides were also coupled with methyl acrylate with lower yields and low palladium leaching.The reverse-phase beads could be recovered from the reaction mixture and were

re-used seven times without any apparent loss of activity.Some reactions could be performed in water or with no added solvent.The real advantage of using the reverse-phase silica support seems to be that more polar substrates can be employed.

The catalysts shown in Chart 1are all stable and active heterogeneous catalysts based on chemically modi?ed silica,prepared by building up a suitable ligand structure,containing an aminopropyl moiety,on the surface of the silica,followed by complexation to the M(II).All of these catalysts have been recently reported and shown to be effective in Heck reactions,complex 1furnished 82%conversion in the coupling of iodobenzene and methyl acrylate with Et 3N in MeCN at 828C for 24h.129This catalyst was successfully re-used without a noticeable loss of activity and with no detectable amounts of palladium leached.The same complex 1,but prepared from PdCl 2instead of Pd(OAc)2on ordered mesoporous silica FSM-16,was active for the coupling of aryl iodides and bromides with methyl acrylate,giving 100%conversion in 1–5h at 1308C.Aryl bromides with electron-donating substituents were particularly sluggish in their reactivity,but the reactivity could be increased by the addition of TBAB.Seven reaction cycles were applied in the vinylation of 4-bromoacetophenone with methyl acrylate without a signi?cant loss of reactivity.130Complex 2was prepared by heating 3-(4,5-dihydroimidazol-1-yl)-propyltriethoxy-silanedichloropalladium(II)with mesoporous silica nano-tube particles.131A 1.5%palladium-imidazoline complex

2

Scheme

33.

Scheme

34.

Chart 1.

F.Alonso et al./Tetrahedron 61(2005)11771–1183511789

with Cs2CO3in dioxane at808C for2–3h gave excellent yields(79–94%)of coupled products obtained for a wide array of bromides or iodides with styrene.In all cases where recycling of the catalyst was attempted,however,small decreases in activity were observed from one run to the next.

A higher reaction temperature(1408C)was required for catalyst3in the reaction of iodobenzene and n-butyl acrylate using sodium carbonate as base in NMP.132High TONs were obtained and the catalyst was recycled three times with high activity,whereas a lower reactivity was observed for styrene,with both E/Z stilbenes being formed in a7:1ratio.A higher loading of catalyst was necessary in the case of4-bromotoluene and a lower yield was found after three runs.Zheng et al.prepared silica-supported poly-g-aminopropylsilane-transition metal complexes4,which were also active and stereoselective for the Heck vinylation reaction of aryl iodides with ole?ns at120–1508C.133All of the complexes were treated with KBH4–EtOH before use. The supported Ni complex furnished the expected products in86–98%yield and the Co and Cu complexes in71–96% yield,although the reaction of iodobenzene and styrene gave stilbene in only40%yield with the latter complexes. An induction period of O2h was observed for these catalysts.The reaction temperature could be reduced by up to70–1008C using a similar,but new,silica-supported poly-g-aminopropylsilane-Cu2C-Pd2C complex.134 Although there is no doubt about the ef?ciency and the possibility of recycling of the above-described catalysts,a comment must be made concerning their preparation.A minimum of three reaction steps are involved in the preparation of the catalysts(10steps for catalyst3)and, in addition,other multiple operations such as?ltration, washing,drying under vacuum or high temperature,or conditioning by re?uxing in a solvent,as well as long reaction times,are needed for some of the steps(up to 4days).Therefore,taking into account the yield reduction when increasing the number of steps,as well as the waste produced along the synthesis of the catalysts and the price of the starting materials and metallic salts,the catalysts4seem to be the most convenient from a practical point of view and for the larger-scale preparations.

In relation to the above catalytic system described by Zheng et al.this research group prepared silica-supported palladium(0)complexes from g-chloropropyl-and g-aminopropyltriethoxysilane via immobilisation on fumed silica,followed by reaction with ethylenediamine and salicylaldehyde and then reaction with PdCl2and reduction with KBH4.135In this case,the reaction temperature was reduced to908C for the Heck reaction of aryl iodides(p-RC6H4I,R Z H,MeO,CO2H)with acrylic acid,methyl acrylate and styrene.The catalysts could be recovered and re-used without loss of activity.A compar-able performance was observed for the silica-supported palladium(0)complex similarly prepared from poly-g-cyanopropyltriethoxysilane.136

N,N-di(pyrid-2-yl)norborn-2-ene-5-ylcarbamide was sur-face grafted or coated onto various silica-based carriers through a ring-opening metathesis polymerisation(ROMP) in the presence of Mo(N-2,6-Me2C6H3)(CHCMe2Ph) [OCMe(CF3)2]2.137The silica-based materials were used in slurry reactions under standard conditions,as well as under microwave irradiation,the latter case leading to a drastic reduction of the reaction times.A quantitative conversion was achieved for iodoarenes,while activated bromoarenes required prolonged reaction times.Typically, less than2.5%palladium was leached into the reaction mixture.Nonetheless,the preparation of the supported catalysts is very sophisticated in order to?nally achieve similar results to those obtained with simpler supported catalytic systems.An example using0.3mol%of the silica-based slurry is depicted in Scheme35.

In1997,Cai et al.described the preparation of a silica-supported poly-g-mercaptopropylsiloxane-palladium(0) complex that gave high yields(86–96%)in the arylation of styrene and acrylic acid(Bu3n N,xylene,1008C,6h)and could be recovered and re-used with a low decrease in activity.138The same ligand,but supported on FSM-16 mesoporous silica,was shown to be an active and stable catalyst for the Heck reaction of4-bromoacetophenone and ethyl acrylate(KOAc,NMP,1308C,92%yield),the catalyst being re-used at least?ve times with no indication of catalyst deactivation.The less reactive electron-rich aryl bromides,4-bromoanisole and bromobenzene,however, resulted in moderate yields(58and62%,respectively), whereas4-chloroacetophenone gave a low yield(18%).139 Based on the above original methodology and,more recently,Cai’s group has prepared a silica-supported bidentate arsine-palladium(0)complex from4-oxa-6,7-dichloroheptyltriethoxysilane via immobilisation on

fumed Scheme35.

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(完整word版)苯基丙酮还原胺化操作工艺的概述与参考

一：苯基丙酮还原胺化介绍： 还原胺化是氨与醛或酮缩合以形成亚胺的过程，其随后还原成胺。利用还原胺化从1-苯基-2-丙酮和氨生产苯丙胺。 氨与醛和酮反应形成称为亚胺的化合物（与消除水的缩合反应）。第一步是亲核加成羰基，随后快速质子转移。所得产物，一种有时称为甲醇胺的hemiaminal通常是不稳定的，不能分离。发生第二反应，其中水从hemiaminal中除去并形成亚胺。 胺随后的还原胺通常通过用氢气和合适的氢化催化剂处理或用铝 - 汞汞齐或通过氰基硼氢化钠处理来完成。 二：苯基丙酮催化氢化还原胺化介绍： 通过醛或酮和氨的混合物的催化氢化进行还原胺化导致存在过量氨时伯胺的优势。应使用至少五当量的氨; 较小的量导致形成更多的仲胺。重要的副反应使还原胺化方法复杂化。当伯胺开始积聚时，它可以与中间体亚胺反应形成还原

成仲胺的亚胺。伯胺也可以与起始酮缩合，得到还原成仲胺的亚胺。通过在反应介质中使用大量过量的氨，可以使该副反应最小化。另一个可能的副反应是将羰基还原成羟基（例如，苯基-2-丙酮可以还原成苯基-2-丙醇）。使用苯基-2-丙酮，甲醇溶剂，阮内镍和在轻微过压下通过溶液鼓泡的氨和氢气的混合物在室温还原胺化下对反应介质进行分析，并将苯丙胺产物经反复结晶。（fn.1）由于苯丙胺中少量的杂质，其中以高得多的量发生杂质的反应混合物用于分析。发现的主要杂质是苯丙胺和苄基甲基酮（苯基-2-丙酮），苄基甲基酮苯基异丙基亚胺的席夫碱（亚胺）。该化合物是未被氢化的苯基-2-丙酮和苯丙胺的缩合产物。还原胺联通通常不会产生非常高的伯胺产率，尽管报告苯丙胺的产率高。阮内镍在这方面特别有用，特别是在升高的温度和压力下。用阮内镍在低压下进行的还原胺化作用通常不是非常成功，除非使用大量的催化剂。应该注意的是，在贵金属的还原胺化中，铵盐的存在是必需的; 在没有铵盐的情况下，催化剂被灭活。亚胺的分离及其随后的还原有时被报道比还原胺化更有效，但是通常难以获得高产量的亚胺和不稳定性，反对该方法。衍生自氨的亚胺倾向于不稳定 - 即使用水也经常迅速水解产生羰基化合物，并且通常易于聚合。 三：苯基丙酮与阮内镍的高压还原胺化工艺步骤：

偶联反应

金属钯催化Sonogashira偶联反应 （芳基炔与芳基卤偶联） 一、实验题目： 金属钯催化Sonogashira偶联反应（芳基炔与芳基卤偶联） 二、实验日期: 实验地点： 实验指导老师： 三、实验目的 1. 学习金属催化的有机偶联反应 2. 掌握Sonogashira偶联的反应机理。 3. 熟练氮气保护、金属催化、回流反应等有机基本操作。 四、实验原理 Sonogashira偶联反应现代有机合成中一种非常重要的形成碳碳键的偶合技术。用于在不饱和碳原子之间形成碳碳单键。 反应是碘代乙烯或芳香烃与端炔之间经催化生成炔烯化合物的反应。反应催化剂为钯和氯化亚铜。反应需要碱性条件下进行。

反应催化循环如下： 钯与碘乙烯发生氧化加成反应，生成乙烯基碘化钯；氯化亚铜在碱性条件下与炔生产炔化铜，后者与乙烯基碘化钯发生金属交换反应，生成乙烯基炔化钯，然后发生还原消除反应生成零价钯和烯炔，完成一个催化循环。 同大多数钯介导的偶合反应一样，该反应一般只适用于不饱和碳原子之间的偶合。在传统有机合成中，乙烯基卤素都是惰性化合物，很难发生取代反应，但在现代有机合成中这种观念发生了彻底的变化。在钯催化下乙烯基卤素化合物变得相当活泼，能发生一系列取代反应。而Sonogashira偶联反应就是其中一个反应代表。烯炔结构是天然产物中常见的结构，特别是菊科植物的次生代谢产物富含这种结构。在全合成研究中Sonogashira偶联反应无疑是一种有力的合成手段。

本次实验是将碘苯和对乙基苯乙炔进行Sonogashira偶联反应，使得苯和碳碳三键直接相连。 反应方程式如下： I CuI,PPh 2 32 + 120C Pd(PPh)Cl 实验装置： 五、实验部分 1、实验仪器：10 mL圆底烧瓶、球形冷凝管、酒精灯、针头、橡胶塞、空气球 2、实验药品：碘代苯、对乙基苯乙炔、碘化亚铜、三乙胺、二氯-二-(三苯基磷）钯

磺化工艺

磺化工艺作业 (一)概念 磺化反应（Sulfonation Reaction）是指有机化合物分子中引入磺酸基（—SO3H）,磺酸盐基（如—SO3Na）或磺酰卤基(—SO2X)的化学反应。引入磺酰卤基的化学反应又可称为卤磺化反应。 根据引入的基团不同，生成的产品可以是磺酸（R-SO3H，R代表烃基）、磺酸盐（R-SO3M，M代表NH4或金属离子）或磺酰卤（R-SO2X，X代表卤素）。根据磺酸基中S原子和有机化合物分子中相连的原子不同得到的产物可以是，与C原子相连的产物为磺酸化合物（R-SO3H）；与O原子相连的产物为硫酸酯（R-OSO3H）；与N原子相连的产物为磺胺化合物（R-NHSO3H）。 重点讨论芳环上的磺化反应。 二、常用磺化剂 ?磺化剂的选择是重要的磺化反应技术之一。常用的磺化剂：硫酸、发烟硫酸、三氧化硫、氯磺酸、硫酰氯、亚硫酸盐等。硫酸是最温和的磺化剂，用于大多数芳香化合物的磺化；氯磺酸是较剧烈的磺化剂，用于磺胺药中间体的制备；三氧化硫是最强的磺化剂，常伴有副产物砜的生成。磺化剂强弱取决于所提供的三氧化硫的有效浓度。 ?（一）硫酸和发烟硫酸 ?1.规格与组成 ?（1）硫酸：是一种无色油状液体，凝固点为10.01℃，沸点为337.85℃(98.3﹪H2SO4) 。 ?（2）工业硫酸：通常有两种规格，即92﹪～93％和98％～100％三氧化硫的一水合物。 ?（3）发烟硫酸：是三氧化硫溶于浓硫酸的产物（H2SO4·xSO3）。

?（4）工业发烟硫酸：通常也制成两种规格，即含游离 ?S O3为20％～25％和60％～65％。 ?3.发烟硫酸作磺化剂的特点 ?(1)反应速度快且稳定，温度较低，同时具有工艺简单、设备投资低、易操作等优点；适用于反应活性较低的芳香化合物磺化和多磺酸物的制备。 ?(2)缺点是其对有机物作用剧烈，常伴有氧化、成砜的副产品。磺化时仍有水产生，生成的水使硫酸浓度下降，当达到95%时反应停止，产生大量的废酸。 3.发烟硫酸作磺化剂的特点 (1)反应速度快且稳定，温度较低，同时具有工艺简单、设备投资低、易操作等优点；适用于反应活性较低的芳香化合物磺化和多磺酸物的制备。 (2)缺点是其对有机物作用剧烈，常伴有氧化、成砜的副产品。磺化时仍有水产生，生成的水使硫酸浓度下降，当达到95%时反应停止，产生大量的废酸。 4.共沸去水磺化法-“气相磺化” (1)原理：将过量的苯蒸汽在120℃～180℃通入浓硫酸中，利用共沸原理使未反应的苯蒸汽带出生成的水，保证硫酸的浓度不致下降太多，这样硫酸的利用率可达91％。 (2)特点：从磺化锅中逸出的苯蒸汽和水蒸汽经冷凝后分层可回收苯，回收的苯经干燥又可循环使用。只适用于沸点较低易挥发的芳烃，例如苯和甲苯的磺化。

suzuki偶联反应

Suzuki-Miyaura交叉偶联反应机理及其在有机合成中的应用 学院：化学学院 专业：有机化学 学号： 姓名：

一、Suzuki-Miyaura 交叉偶联反应概念 Suzuki 反应（铃木反应），也称作Suzuki 偶联反应、Suzuki-Miyaura 反应（铃木－宫浦反应），是一个较新的有机偶联反应，是在钯配合物催化下，芳基或烯基的硼酸或硼酸酯与氯、溴、碘代芳烃或烯烃发生交叉偶联。 Z=Cl,Br,I 自从1981年Suzuki 等报道了通过钯催化的有机硼化学物和卤代烃可以在很温和的条件下发生偶联反应制备不对称联芳烃以后，为芳-芳键的形成展开了一个新的领域[1]。Suzuki-Miyaura 交叉偶联反应被证明是目前制备联芳基及其衍生物最为广泛利用的方法，因为其具有很强的底物适应性及官能团耐受性，常用于合成多烯烃、苯乙烯和联苯的衍生物，从而应用于众多天然产物、有机材料的合成中。铃木章也凭借此贡献与理查德·赫克、根岸英一共同获得2010年诺贝尔化学奖。 二、Suzuki-Miyaura 交叉偶联反应机理 Suzuki-Miyaura 交叉偶联的反应机理通常是一个普通的催化循环过程。这个过程主要包括三个步骤： （1）氧化加成(oxidative addition) （2）转移金属化(transmetalation) （3）还原消除(reductive elimination) Ar-Pd-Ar 1 Ar-Ar Pd(0) ArX ArPdX ArPdOH NaOH NaX B(OH)4 ArB -(OH)3 NaOH ArB(OH)2 氧化加成 还原消除 转移金属化 Z B(OH)2 Br Z + 3% Pd(PPh 3)4Benzene, Na 2CO 3/H 2O

磺化反应

磺化反应 ●概述 ●磺化剂的种类 ●磺化反应历程 ●磺化反应的影响因素 ●磺化方法 ●磺化后处理 一、概述 1，目的 Ar-H + H2SO4 → Ar-SO3H ①使产物具有水溶性、酸性、表面活性或对纤维的亲和力如产物表面活性 ②将-SO3H 转变为-OH,-NH2,-CN,-X等，从而制成系列中间体基团置换§2.1概述 ③利用磺酸基的水解性，完成特定的反应后，再将其水解安定蓝B 色基 2，磺化方法（引入SO3H的方法） 过量硫酸法 共沸去水法（溶剂法） 三氧化硫法 氯磺酸（Cl SO3H ）磺化法 亚硫酸盐磺化法（NaHSO3）

二、磺化剂的种类 1，SO 3---最有效的磺化剂SO3 2，H 2SO 4和发烟硫酸H2SO4和发烟硫酸 3，氯磺酸氯磺酸 4，亚硫酸钠或亚硫酸氢钠 三、磺化反应历程 ● 磺化动力学 ● 反应历程 1、 磺化动力学 可能的磺化质点是不同溶剂化的SO 3分子 , a, 在发烟硫酸中主要的磺化质点为SO 3， b, 在较浓的硫酸中的质点为H 2S 2O 7，它是SO 3和H 2SO 4溶剂化的形式 C,在较低浓度的硫酸中（80％－85％）主要是H 3SO 4＋，它是SO 3和H 3O ＋溶剂化形式 磺化反应动力学 SO 3+H 2SO 4 H 2S 2O 7SO 3 + H 3O + H 3SO 4 + 133333] ][)[()(SO ArH SO k SO v H ArSO SO ArH K k =?→←+- +

2、反应历程 四、磺化反应的影响因素 ●被磺化有机物的性质 ●磺基的水解 ●磺化温度 ●磺化剂的浓度和用量 ●添加剂的影响 1、被磺化物的性质

实验室常用的几个反应机理必需掌握

Negishi偶联反应 偶联反应，也写作偶合反应或耦联反应，是两个化学实体（或单位）结合生成一个分子的有机化学反应。狭义的偶联反应是涉及有机金属催化剂的碳-碳键形成反应，根据类型的不同，又可分为交叉偶联和自身偶联反应。在偶联反应中有一类重要的反应，RM（R = 有机片段, M = 主基团中心）与R'X的有机卤素化合物反应，形成具有新碳-碳键的产物R-R'。[1]由于在偶联反应的突出贡献，根岸英一、铃木章与理查德·赫克共同被授予了2010年度诺贝尔化学奖。[2] 偶联反应大体可分为两种类型： ?交叉偶联反应：两种不同的片段连接成一个分子，如：溴苯 (PhBr)与氯 )。 乙烯形成苯乙烯(PhCH=CH 2 ?自身偶联反应：相同的两个片段形成一个分子，如：碘苯 (PhI)自身形成联苯 (Ph-Ph)。 反应机理 偶联反应的反应机理通常起始于有机卤代烃和催化剂的氧化加成。第二步则是另一分子与其发生金属交换，即将两个待偶联的分子接于同一金属中心上。最后一步是还原消除，即两个待偶联的分子结合在一起形成新分子并再生催化剂。不饱和的有机基团通常易于发生偶联，这是由于它们在加合一步速度更快。中间体通常不倾向发生β-氢消除反应。[3] 在一项计算化学研究中表明，不饱和有机基团更易于在金属中心上发生偶联反应。[4]还原消除的速率高低如下： 乙烯基－乙烯基 > 苯基－苯基 > 炔基－炔基 > 烷基－烷基 不对称的R-R′形式偶联反应，其活化能垒与反应能量与相应的对称偶联反应 R-R与R′-R′的平均值相近，如：乙烯基－乙烯基 > 乙烯基－烷基 > 烷基－烷基。 另一种假说认为，在水溶液当中的偶联反应其实是通过自由基机理进行，而不是金属－参与机理。 催化剂 偶联反应中最常用的金属催化剂是钯催化剂，有时也使用镍与铜催化剂。钯催化剂当中常用的如：四(三苯基膦)钯等。钯催化的有机反应有许多优点，如：官能团的耐受性强，有机钯化合物对于水和空气的低敏感性。

磺化聚苯乙烯型阳离子交换树脂的制备与性能研究(DOC)

功能高分子材料课程论文 磺化聚苯乙烯型阳离子交换树脂的制 备与性能研究 专业：材料工程系 学生姓名： 班级： 学号： 完成时间：2013年1月7 日

摘要 介绍了磺化聚苯乙烯（SPS）型离子交换树脂的合成方法；综述了近年来在氯甲基化反应、Mannich反应以及磺化反应上的新进展、新理论；从结构上对聚苯乙烯型离子交换树脂的强度和热稳定性进行了分析。聚苯乙烯型离子交换树脂具有稳定的物理化学性质、吸附选择独特、再生容易、操作简便、使用周期长等优良性能，大大促进了化工企业、制药工业、环保、医疗、分析等行业的发展，具有广阔的发展前景。 关键词聚苯乙烯型离子交换树脂；苯乙烯；二乙烯苯；浓硫酸；磺化

目录 1 磺化聚苯乙烯型阳离子交换树脂的合成 (4) 1.1目的要求 (4) 1.2 原理 (4) 1.3所需仪器、药品 (5) 1.4实验步骤 (5) 2 磺化聚苯乙烯型阳离子交换树脂的性能研究 (6) 2.1 SPS的结构分析 (7) 2.2硫酸的用量对SPS磺化度的影响 (7) 2.3磺化度对离子交换容量(IEC)的影响 (8) 2.4磺化度对SPS电导率的影响 (9) 2.5SPS溶液的特性粘数 (9) 3 结论 (10) 参考文献 (11) 致谢 (12)

离子交换树脂由加聚型到聚苯乙烯型的转变是一个质的飞跃。在合成离子交换树脂的初期，主要是以加聚型为主，但是合成的树脂难以成球状并且化学稳定性较差，机械强度不好，在使用过程中常有可溶性物质渗出。 磺化聚苯乙烯树脂以聚苯乙烯为骨架，与小分子的功能基以化学键的形式结合，因此既保留了原有低分子的各种优良性能，又由于高分子效应可增添新的功能，这使得离子交换树脂的性能大幅度提高，品种成倍地增加，应用范围迅速扩大，大大促进了化工企业、制药工业、环保等行业的发展，对世界经济、政治、军事的发展产生了巨大的影响。因此，在高分子材料达到分子设计水平的今天，了解离子交换树脂的合成原理，研究离子交换树脂的结构和性能很有意义。 1.0磺化聚苯乙烯型阳离子交换树脂的合成 1.1目的要求 1.1.1熟悉悬浮聚合方法 1.1.2通过共聚物的磺化反应，了解高分子化学反应的一般概念。 1.1.3掌握离子交换树脂的净化和交换当量的测定 1.2原理 离子交换树脂是一种具有离解能力的高聚物，它一般包括两部分组成，一是具有体型网状结构的母体骨架，一是在母体骨架上的可离解基团（官能团），这种可离解基团能和溶液中的离子起交换反应。如 l-M-SO 3 -Na+ + H+Cl- M-N+(CH 3) 3 OH- M-SO 3-H+ + Na+C+ Na+Cl- M-N+(CH 3 ) 3 Cl- + Na+OH- 式中：M代表树脂母体骨架。 本实验是由苯乙烯和二乙烯苯以悬浮聚合获得共聚物小球（即母体骨架），然后用浓硫酸磺化为强酸型阳离子交换树脂。其反应为：

偶联反应一览表

反应名称发现 年代 反应物A反应物B 类 型 催化 剂 备 注 武兹反应（Wurtz reaction）1855 R-X sp3R-X sp3 自 身 以 Na 消 除 反 应 物 的 卤 原 子 格拉泽偶联反应（Glaser coupling）1869 RC≡CH sp RC≡CH sp 自 身 Cu 氧 气 作 为H 受 体 乌尔曼反应（Ullmann reaction）1901 Ar-X sp2Ar-X sp2 自 身 Cu 高 温 冈伯格-巴克曼反应1924 Ar-H sp2Ar-N2X sp2自 身 需 碱 参 与 Cadiot-Chodkiewicz 偶联反应1957 RC≡CH sp RC≡CX sp 交 叉 Cu 需 碱 参 与 Castro-Stephens偶联反应1963 RC≡CH sp Ar-X sp2 交 叉 Cu 吉尔曼试剂偶联反应 （Gilman reagent coupling）1967 R2CuLi R-X 交 叉 Cassar反应1970 烯烃sp2R-X sp3交 叉 Pd 需 碱 参 与 熊田偶联反应（Kumada coupling）1972 Ar-MgBr sp2, sp3 Ar-X sp2 交 叉 Pd or

Ni 赫克反应（Heck reaction）1972 烯烃sp2R-X sp2 交 叉 Pd 需 碱 参 与 薗头偶联反应 （Sonogashira coupling）1975 RC≡CH sp R-X sp3 sp2 交 叉 Pd and Cu 需 碱 参 与 根岸偶联反应（Negishi coupling）1977 R-Zn-X sp3, sp2, sp R-X sp3 sp2 交 叉 Pd or Ni 施蒂勒反应（Stille coupling）1978 R-SnR3 sp3, sp2, sp R-X sp3 sp2 交 叉 Pd 铃木反应（Suzuki reaction）1979 R-B(OR)2sp2R-X sp3 sp2 交 叉 Pd 需 碱 参 与 Hiyama偶联反应1988 R-SiR3sp2R-X sp3 sp2 交 叉 Pd 需 碱 参 与 Buchwald–Hartwig 偶联反应1994 R2N-R SnR3sp R-X sp2 交 叉 Pd N-C 偶 联 反 应 福山偶联反应 （Fukuyama coupling）1998 RCO(SEt) sp2R-Zn-I sp3交 叉 Pd

胺的合成反应综述

Studies in Synthetic Chemistry 合成化学研究, 2016, 4(2), 11-18 Published Online June 2016 in Hans. https://www.wendangku.net/doc/7e2513454.html,/journal/ssc https://www.wendangku.net/doc/7e2513454.html,/10.12677/ssc.2016.42002 文章引用: 何永富, 李荣疆. 胺的合成反应综述[J]. 合成化学研究, 2016, 4(2): 11-18. The Summary of the Synthesis of Amines Yongfu He, Rongjiang Li Hangzhou Yuanchang Pharmaceutical Sci-Tech Co., Ltd., Hangzhou Zhejiang Received: Sep. 30th , 2016; accepted: Oct. 16th , 2016; published: Oct. 19th , 2016 Copyright ? 2016 by authors and Hans Publishers Inc. This work is licensed under the Creative Commons Attribution International License (CC BY). https://www.wendangku.net/doc/7e2513454.html,/licenses/by/4.0/ Abstract Amines, as a class of very effective drug functional groups, exist on most pharmaceutical struc-tures. In this paper, we summarize the main methods for the synthesis of existing amines, and ex-plore the methods for the synthesis of novel amines. Keywords Amine, Amino, Synthesis of Amines 胺的合成反应综述 何永富，李荣疆 杭州源昶医药科技有限公司，浙江 杭州 收稿日期：2016年9月30日；录用日期：2016年10月16日；发布日期：2016年10月19日 摘 要 胺作为一类非常有效的药物官能团，存在于大多数药物结构之上。本文总结现有胺的合成的主要方法，以及探索寻找新的胺的合成方法。 Open Access

偶联反应及举例

偶联反应[编辑] 偶联反应，也写作偶合反应或耦联反应，是两个化学实体（或单位）结合生成一个分子的有机化学反应。狭义的偶联反应是涉及有机金属催化剂的碳-碳键形成反应，根据类型的不同，又可分为交叉偶联和自身偶联反应。在偶联反应中有一类重要的反应，RM（R = 有机片段, M = 主基团中心）与R'X的有机卤素化合物反应，形成具有新碳-碳键的产物R-R'。[1]由于在偶联反应的突出贡献，根岸英一、铃木章与理查德·赫克共同被授予了2010年度诺贝尔化学奖。[2] 偶联反应大体可分为两种类型： ?交叉偶联反应：两种不同的片段连接成一个分子，如：溴苯 (PhBr)与氯乙烯形成苯乙烯(PhCH=CH2)。 ?自身偶联反应：相同的两个片段形成一个分子，如：碘苯 (PhI)自身形成联苯 (Ph-Ph)。 反应机理[编辑] 偶联反应的反应机理通常起始于有机卤代烃和催化剂的氧化加成。第二步则是另一分子与其发生金属交换，即将两个待偶联的分子接于同一金属中心上。最后一步是还原消除，即两个待偶联的分子结合在一起形成新分子并再生催化剂。不饱和的有机基团通常易于发生偶联，这是由于它们在加合一步速度更快。中间体通常不倾向发生β-氢消除反应。[3] 在一项计算化学研究中表明，不饱和有机基团更易于在金属中心上发生偶联反应。[4]还原消除的速率高低如下： 乙烯基－乙烯基> 苯基－苯基> 炔基－炔基> 烷基－烷基 不对称的R-R′形式偶联反应，其活化能垒与反应能量与相应的对称偶联反应R-R与R′-R′ 的平均值相近，如：乙烯基－乙烯基> 乙烯基－烷基> 烷基－烷基。 另一种假说认为，在水溶液当中的偶联反应其实是通过自由基机理进行，而不是金属－参与机理。[5] §催化剂[编辑] 偶联反应中最常用的金属催化剂是钯催化剂，有时也使用镍与铜催化剂。钯催化剂当中常用的如：四(三苯基膦)钯等。钯催化的有机反应有许多优点，如：官能团的耐受性强，有机钯化合物对于水和空气的低敏感性。 如下一些关于钴催化的偶联反应的综述[6]，钯[7][8][9][10][11]和镍[12]介导的反应以及它们的应用[13][14]。 §离去基团[编辑] 离去基团X在有机偶联反应中，常常为溴、碘或三氟甲磺酰基。较理想的离去基团为氯，因有机氯化合物相对其他的这些离去基团更廉价易得。与之反应的有机金属化合物还有锡、锌或硼。 §操作条件[编辑]

芳胺化反应-经典化学合成反应标准操作

经典化学合成反应标准操作 芳胺化反应 目录 一．前言 (1) 二．影响Buchwald 反应的因素及Buchwald 反应的应用 (2) 2.1 卤素对反应的影响............................................................................................................ 2.2 取代基团电子性对反应的影响....................................................................................... 2.3 配体对反应的影响............................................................................................................ 2.4 胺与苯基三氟甲磺酸酯的反应（Triflate） ................................................................. 2.5 对伯胺及仲胺的选择性.................................................................................................... 2.6 对手性的影响 .................................................................................................................... 2.7 与吡咯及吲哚的反应........................................................................................................ 2.8 关环反应............................................................................................................................. 2.9 卤代苯转化为苯胺反应.................................................................................................... 三．反应操作示例.............................................................................................. 3.1 典型操作一 ........................................................................................................................ 3.2 典型操作二 ........................................................................................................................ 四、参考文献 .....................................................................................................

偶联反应

偶联反应 目录 偶联反应 常见的偶联反应包括 偶联反应具体说明 偶联反应所需要注意的 用途 Suzuki反应 偶联反应 偶联反应（英文：Coupled reaction），也作偶连反应、耦联反应、氧化偶联，是由两个有机化学单位（molecules）进行某种化学反应而得到一个有机分子的过程.这里的化学反应包括格氏试剂与亲电体的反应 偶联反应 (Grinard），锂试剂与亲电体的反应，芳环上的亲电和亲核反应（Diazo,Addition-Elimination），还有钠存在下的Wutz反应，由于偶联反应 (Coupled Reaction）含义太宽，一般前面应该加定语.而且这是一个比较非专业化的名词. 狭义的偶联反应是涉及有机金属催化剂的碳-碳键生成反应，根据类型的不同，又可分为交叉偶联和自身偶联反应。进行偶联反应时，介质的酸碱性是很重要的。一般重氮盐与酚类的偶联反应，是在弱碱性介质中进行的。在此条件下，酚形成苯氧负离子，使芳环电子云密度增加，有利于偶联反应的进行。重氮盐与芳胺的偶联反应，是在中性或弱酸性介质中进行的。在此条件下，芳胺以游离胺形式存在，使芳环电子云密度增加，有利于偶联反应进行。如果溶液酸性过强，胺变成了铵盐，使芳环电子云密度降低，不利于偶联反应，如果从重氮盐的性质来看，强碱性介质会使重氮盐转变成不能进行偶联反应的其它化合物。偶氮化合物是一类有颜色的化合物，有些可直接作染料或指示剂。在有机分析中，常利用偶联反应产生的颜色来鉴定具有苯酚或芳胺结构的药物。 常见的偶联反应包括 反应名称－－年代－－反应物A－－反应物B －－类型－－催化剂－－注 Wurtz反应 1855 R-X sp³ 自身偶联 Na Glaser偶联反应 1869 R-X sp 自身偶联 Cu Ullmann反应 1901 R-X sp² 自身偶联 Cu Gomberg-Bachmann反应 1924 R-N2X sp² 自身偶联以碱作介质

偶联反应总结

反应名称－－年代－－反应物A－－反应物B －－类型－－催化剂－－注 Wurtz反应1855 R-X sp³ 自身偶联Na Glaser偶联反应1869 R-X sp自身偶联Cu Ullmann反应1901 R-X sp² 自身偶联Cu Gomberg-Bachmann反应1924 R-N2X sp² 自身偶联以碱作介质 Cadiot-Chodkiewicz偶联反应1957炔烃sp R-X sp交叉偶联Cu 以碱作介质 Castro-Stephens偶联反应1963 R-Cu sp R-X sp² 交叉偶联 Kumada偶联反应1972 R-MgBr sp²；、sp³ R-X sp² 交叉偶联Pd 或Ni Heck反应1972烯烃sp² R-X sp² 交叉偶联Pd以碱作介质 Sonogashira偶联反应1973炔烃sp R-X sp³ sp² 交叉偶联Pd、Cu 以碱作介质 Negishi偶联反应1977 R-Zn-X sp² R-X sp³ sp² 交叉偶联Pd或Ni Stille偶联反应1977 R-SnR3 sp² R-X sp³ sp² 交叉偶联Pd Suzuki反应1979 R-B(OR)2 sp² R-X sp³ sp² 交叉偶联Pd以碱作介质 Hiyama偶联反应1988 R-SiR3 sp² R-X sp³ sp² 交叉偶联Pd以碱作介质 Buchwald-Hartwig反应1994 R2N-R SnR3 sp R-X sp² 交叉偶联Pd N-C偶联Fukuyama偶联反应1998 RCO(SEt) sp2 R-Zn-I sp3 交叉偶联Pd

还原胺化

如楼上所说,纯化每一步是关键的,不纯化直接往下投反应,虽然做的很快,但是一旦某个环节出了问题,就会很难发现问题出在哪.第一步要纯化一下,哪怕过个柱子,第二步还原胺化反应,建议用1,2-二氯乙烷做溶剂反应体系中加醋酸催化,另加无水MgSO4,或者活化的分子筛.量大的化直接亚胺也行,用甲苯做溶剂,分 水器分水,最后反应体系无需后处理,直接加入NaBH(CN)3还原.NaBH(CN)3还原的好处就是只还原亚胺,不还原醛基(书本知识,没有试过,不过听同事也是这么说的,我相信他们做过),这样有利于分离纯化.因为吡啶甲醇的极性不会小,做过有点体会.这步做纯了,下步掉Boc就没有问题了. 2.你的问题主要是还原胺化这步，我做一系列的还原胺化，觉得下面的这个条件可以通用：胺一个当量，醛4个当量，加点醋酸，甲醇作溶剂，加三个当量的氰基硼氢化钠，常温反应就可以了。 ）这个反应中的亚胺大部分相当不稳定，和原料是平衡的。生成了，也检测不准。我们做都不检测 2）酸性有利于加快还原速度，但pH要大于5 3）溶剂，试剂最好无水 4）三乙酰氧基硼氢化钠分批加 5)最好通氮气隔绝空气和水 6）)这个反应用四氢呋喃做溶剂的多，二氯甲烷也可以。 我刚做过一个还原胺化的优化，在甲醇中做的，有少量水存在对收率影响不大，但溶剂中水量增加会对反应有影响，增加到50%就完全得不到产物了。得到的是一个副产物，因为是氨基酸溶解度不好没做核磁，不知道结构。但肯定不是原料。 DCM or DCE做溶剂，加入2.0~3.0eq 乙醛+0.1eq 醋酸催化室温搅拌 2. 等肼完全转化为亚胺之后，加入NaCNBH3 or Na（OAc)3BH 室温搅拌。。。。。。。。 哪怕过个柱子,第二步还原胺化反应,建议用1,2-二氯乙烷做溶剂反应体系中加醋酸催化,另加无水MgSO4,或者活化的分子筛.量大的化直接亚胺也行,用甲苯 做溶剂,分水器分水,最后反应体系无需后处理,直接加入NaBH(CN)3还 原.NaBH(CN)3还原的好处就是只还原亚胺,不还原醛基(书本知识,没有试过,不

还原胺化反应的新进展

2007年第27卷有机化学V ol. 27, 2007第1期, 1～7 Chinese Journal of Organic Chemistry No. 1, 1～7 * E-mail: wangdq@https://www.wendangku.net/doc/7e2513454.html, Received December 8, 2005; revised March 20, 2006; accepted May 8, 2006.

2 有 机 化 学 V ol. 27, 2007 合成中得到广泛应用[2]. 最近Blechert 等[3]报道了多官能团化合物1在Pd/C 催化氢化条件下“一锅”完成双键还原、酮羰基还原胺化、醛的脱保护、醛的还原胺化、苄氧羰基的脱除5步反应形成双环哌啶并吡咯啉化合物2 (Eq. 1). 除了Pd 以外, 其它金属如Ni, Pt 等也被用作氢化胺化催化剂. Nugent 等[4]报道了在烷氧钛的存在下, 不对称烷基酮与(R )-1-甲基苄胺(MBA)反应, Raney-Ni 催化氢化产生立体选择性非常高的二级胺3, 然后Pd/C 催化氢解给出收率和旋光性比较好的一级胺4 (71%～78%收率, 72%～98% ee ) (Scheme 1). 同样如果烷基酮与 (S )-MBA 反应、氢解可以得到与3和4相反构型的胺. 该方法尽管从酮开始需要两步反应产生手性一级胺, 但试剂价廉易得, 有利于规模化生产 . Scheme 1 1.2 金属络合物催化还原胺化 金属络合物在催化氢化方面具有优异的催化活性, 而且比仅用金属催化氢化具有更好的选择性. Beller 等[5]报道了0.05 mol%的[Rh(cod)Cl]2与TPPTS (tris so-dium salt of meta trisulfonated triphenylphosphine)形成络合物催化各种醛与氨的还原胺化, 得到高收率的胺化产物(最高97%) (Eq. 2). Rh 络合物易溶于水, 反应可在水溶液中进行 . Angelovski 等[6]应用0.5 mol%的[Rh(acac)(CO)2]催化氢化大环二醛与二胺形成大环二胺, 收率57%～76%, 而用其它还原胺化试剂[NaBH 3CN, NaB(AcO)3H]只得到 不超过30%收率的产物. Rh 络合物在参与关环过程中具有更好的模板效应. 2005年, Ohta [7]报道了以离子液体咪唑盐7为反应介质, 2 mol% [Ir(cod)2]BF 4进行的直接还原胺化, 不需任何配体的参与, 往离子液体中通入一定压力氢气, 获得收率79%～99%的二级胺(Eq. 3). 离子液体的阴离子部分对反应影响很大, 以[Bmim]BF 4为介质时收率最好. 氢气压力增大、温度升高有利于反应速率和收率的提高 . 天然含有胺基的化合物(吗啡、麻黄碱、氨基酸等)往往都是光活性的, 手性胺基的获得有着更重要的意义, 也是该领域研究的热点. 由醛(酮)直接或间接还原胺化为立体专一异构体是获得手性胺基化合物的重要途径. 目前已报道的是手性过渡金属络合物不对称催化还原亚胺[8], 其中以Ir, Rh 和Ru 与手性配体形成的络合物进行的不对称还原胺化较为常见. 2004年Andersson [9]报道了Ir 的络合物催化亚胺还原胺化反应(Eq. 4). 由酮与胺反应, 经过亚胺8, 然后被膦-噁唑啉与铱的络合物10进行催化氢化, 可得R 型为主的手性胺9 . Kadyrov 等[10]报道了同样的反应, 以[(R )-tol-binap]- RuCl 2为催化剂对芳香酮的还原胺化, 得到84% ee 的R -异构体, 而对脂肪酮的反应, 对映选择性一般低于30%. 由酮与胺形成亚胺, 不需分离直接进行还原是更简单实用的方法, 然而成功的报道为数不多[11]. 2003年, Zhang 等[12]报道了在Ti(OPr-i )4存在下, Ir-f-Binaphane (14)催化氢化各种芳香酮与对甲氧苯胺的还原胺化, 取得收率和对映选择性都非常好的结果(最低93%收率, 最高96% ee ), 其反应过程见Scheme 2. 首先在Lewis 酸

还原胺化反应综述

Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride.Studies on Direct and Indirect Reductive Amination Procedures1 Ahmed F.Abdel-Magid,*Kenneth G.Carson,Bruce D.Harris,Cynthia A.Maryanoff,and Rekha D.Shah The R.W.Johnson Pharmaceutical Research Institute,Department of Chemical Development, Spring House,Pennsylvania19477 Received January8,1996X Sodium triacetoxyborohydride is presented as a general reducing agent for the reductive amination of aldehydes and ketones.Procedures for using this mild and selective reagent have been developed for a wide variety of substrates.The scope of the reaction includes aliphatic acyclic and cyclic ketones,aliphatic and aromatic aldehydes,and primary and secondary amines including a variety of weakly basic and nonbasic amines.Limitations include reactions with aromatic and unsaturated ketones and some sterically hindered ketones and amines.1,2-Dichloroethane(DCE)is the preferred reaction solvent,but reactions can also be carried out in tetrahydrofuran(THF)and occasionally in acetonitrile.Acetic acid may be used as catalyst with ketone reactions,but it is generally not needed with aldehydes.The procedure is carried out effectively in the presence of acid sensitive functional groups such as acetals and ketals;it can also be carried out in the presence of reducible functional groups such as C-C multiple bonds and cyano and nitro groups.Reactions are generally faster in DCE than in THF,and in both solvents,reactions are faster in the presence of AcOH.In comparison with other reductive amination procedures such as NaBH3CN/MeOH,borane-pyridine, and catalytic hydrogenation,NaBH(OAc)3gave consistently higher yields and fewer side products. In the reductive amination of some aldehydes with primary amines where dialkylation is a problem we adopted a stepwise procedure involving imine formation in MeOH followed by reduction with NaBH4. Introduction The reactions of aldehydes or ketones with ammonia, primary amines,or secondary amines in the presence of reducing agents to give primary,secondary,or tertiary amines,respectively,known as reductive aminations(of the carbonyl compounds)or reductive alkylations(of the amines)are among the most useful and important tools in the synthesis of different kinds of amines.The reaction involves the initial formation of the intermediate carbinol amine3(Scheme1)which dehydrates to form an imine.Under the reaction conditions,which are usually weakly acidic to neutral,the imine is protonated to form an iminium ion4.2Subsequent reduction of this iminium ion produces the alkylated amine product5. However,there are some reports that provide evidence suggesting a direct reduction of the carbinol amine3as a possible pathway leading to5.3The choice of the reducing agent is very critical to the success of the reaction,since the reducing agent must reduce imines (or iminium ions)selectively over aldehydes or ketones under the reaction conditions. The reductive amination reaction is described as a direct reaction when the carbonyl compound and the amine are mixed with the proper reducing agent without prior formation of the intermediate imine or iminium salt.A stepwise or indirect reaction involves the prefor-mation of the intermediate imine followed by reduction in a separate step. The two most commonly used direct reductive amina-tion methods differ in the nature of the reducing agent. The first method is catalytic hydrogenation with plati-num,palladium,or nickel catalysts.2a,4This is an economical and effective reductive amination method, particularly in large scale reactions.However,the reac-tion may give a mixture of products and low yields depending on the molar ratio and the structure of the reactants.5Hydrogenation has limited use with com-pounds containing carbon-carbon multiple bonds and in the presence of reducible functional groups such as nitro6,7and cyano7groups.The catalyst may be inhibited by compounds containing divalent sulfur.8The second method utilizes hydride reducing agents particularly sodium cyanoborohydride(NaBH3CN)for reduction.9The successful use of sodium cyanoborohydride is due to its stability in relatively strong acid solutions(～pH3),its solubility in hydroxylic solvents such as methanol,and its different selectivities at different pH values.10At pH X Abstract published in Advance ACS Abstracts,May1,1996. (1)Presented in part at the33rd ACS National Organic Symposium, Bozeman,Mo,June1993,Paper A-4.Preliminary communications:(a) Abdel-Magid,A.F.;Maryanoff,C.A.;Carson,K.G.Tetrahedron Lett. 1990,31,5595.(b)Abdel-Magid,A.F.;Maryanoff,C.A.Synlett1990, 537. (2)The formation of imines or iminium ions was reported as possible intermediates in reductive amination reactions in catalytic hydrogena-tion methods,see(a)Emerson,https://www.wendangku.net/doc/7e2513454.html,.React.1948,4,174and references therein.It was also proposed in hydride methods,see(b) Schellenberg,https://www.wendangku.net/doc/7e2513454.html,.Chem.1963,28,3259. (3)Tadanier,J.;Hallas,R.;Martin,J.R.;Stanaszek,R.S.Tetra-hedron1981,37,1309 (4)(a)Emerson,W.S.;Uraneck,C.A.J.Am.Chem.Soc.1941,63, 749.(b)Johnson,H.E.;Crosby,https://www.wendangku.net/doc/7e2513454.html,.Chem.1962,27,2205. (c)Klyuev,M.V.;Khidekel,M.L.Russ.Chem.Rev.1980,49,14. (5)Skita,A.;Keil,F.Chem.Ber.1928,61B,1452. (6)Roe,A.;Montgomery,J.A.J.Am.Chem.Soc.1953,75,910. (7)Rylander,P.N.In Catalytic Hydrogenation over Platinum Metals;Academic Press,New York,1967;p128. (8)Rylander,P.N.In Catalytic Hydrogenation over Platinum Metals;Academic Press,New York,1967;p21. (9)For a recent review on reduction of C d N compounds with hydride reagents see:Hutchins,R.O.,Hutchins,M.K.Reduction of C d N to CHNH by Metal Hydrides.In Comprehensive Organic Synthesis;Trost, B.N.,Fleming,I.,Eds.;Pergamon Press:New York,1991;Vol.8. 3849 https://www.wendangku.net/doc/7e2513454.html,.Chem.1996,61,3849-3862 S0022-3263(96)00057-6CCC:$12.00?1996American Chemical Society