Chapter 8. Reactions Involving the Transition Metals Introduction Main group metals are used in stoichiometric reaction, but many of transition metal are used in catalytic process. Transition metals frequently involve oxidation state changes at the metal 8.1 Organocopper Intermediates Preparatioon and structure of Organocopper reagents.

catalytic amount1,4-addition reaction 1,2-addition reaction The 2:1 species are known as cuprates and are the most important as synthetic reagents.

In solution, lithium dimethylcuprate exists as a dimer, [LiCu(CH 3 ) 2 ] 2. Four methyl groups are attached to a tetrahedral cluster of lithium and copper atoms. However, in the presence of LiI, the compound seems to be a monomer of compostition (CH 3 ) 2 CuLi. Cuprates with two different copper substituents have been developed (Table 8.1).

An important type of mixed cuprates is prepared from a 2:1 ratio of an alkyllithium and CuCN: higher-order cyanocuprates. Same reactivity, but more stable than dialkyl cuprate. R 2 CuCNLi 2 in THF CN doesn’t seem to be bound directly to the copper. Only one of two organic groups is tranferred. 2-thienyl group is not tranferred. Selectively transfer the alkenyl group in conjugate addition reaction

Metal-metal exchange reaction Reactions Involving Orgnocopper Reagents and Intermediates Organocopper reagents: nucleophilic displacements on halides and sulfonates. Epoxide ring opening, conjugate additions to  -unsaturated carbonyl compounds, and additions to alkynes.

The addition of halides to transition-metal species with low oxidation states is a common reaction in transition-metal chemistry and is called oxidative addition. The formal oxidation state of copper after addition is 3+. This step is followed by combination of two of the alkyl groups from copper: reductive elimination. Allylic halide give both S N 2 products and products of substitution with and allylic shift (S N 2’ products) although the mixed organocopper reagent RCu-BF 3 is reported to give mainly the S N 2’ product.

The reaction shows a preference for anti stereochemistry in cyclic systems. Propargyl acetates, halides, and sulfonates also react with a double-bond shift to give allenes.

Halogens  to carbonyl groups can be successfully coupled with organocopper Reagents. Introduced at less hindered carbon of the epoxide ring.

The addition is accelerated by trimethylsilyl choride or a combination of trimethylsilyl chloride and HMPA. The rate enhancement is attributed to trapping or a reversibly formed complex between the enone and cuprate. The efficiency of the reaction is improved by the addition of trialkylphosphines to the reaction mixture.

The lithium ion also plays a key role, presumably by Lewis acid coordination at the carbonyl oxygen. Isotope effects indicate that the collapse of the adduct by reductive elimination is the rate determining step. The more easily reduced, the more reactive is the compound toward cuprate reagents. Compounds such as  -unsaturated esters and nitriles, which are not as easily reduced as the corresponding ketones, do not react as readily with dialkyl cuprates, even though they are good Michael acceptors in classical Michael reactions with carbanions.

In the presence of LiI, TMS-Cl, and catalystic amount of (CH 3 ) 2 Cu(CN)Li 2, conjugate addition of organozinc reagents occurs in good yield. Simple organozinc reagents undergo conjugate addition with CuO 3 SCF 3 as catalyst in the presence of phosphines or phosphites.

Conjugate addition reactions involving organocopper intermediates can be made enantioselective by using chiral ligands.

Conjugate addition to  -unsaturated esters can often be effected by copper catalyzed reaction with Grignard reagent. Other reactions, such as epoxide ring opening, can also be carried out under catalytic conditions. (Scheme 8.5)

Conjugate acetylenic esters react readily with cuprate reagents, with syn addition being kinetically preferred. Mixed copper-magnesium reagents analogous to the lithium cuprates can be prepared. These compounds are often called Normant reagents. The reagents undergo addition to terminal alkynes to generate alkenylcopper reagents. The addition is stereospecifically syn. protonolysis

Organocopper intermediates are also involved in several procedures for coupling of two organic reactants to form a new carbon-carbon bond. Classical example of this type of reaction is the Ullman coupling, which is done by heating an aryl halide with a copper-bronze alloy. Good yields by this method are limited to halides with electron-attracting substituents.

Arylcopper intermediates can be generated from organolithium compounds as in the preparation of cuprates. These compounds react with a second aryl halide to provide unsymmetrical biaryls.

8.2 Reactions Involving Organopallasium Intermediates Catalytic processes have both economic and environmental advantage. Three types of organopalladium intermediates are of primary importance in the reactions that have found synthetic application. Palladium can be replaced by hydrogen under reductive conditions In the absence of a reducing reagent, an elimination of Pd(0) and a proton occurs.

A second type of organopalladium intermediates are  -allyl complexes. These complexes can be obtained from Pd(II) salts and allyl acetates and other compounds with potential leaving groups in an allylic poistion. The  -allyl complexes can be isolated as halide-bridged dimers.

The third general process involves the reaction of Pd(0) species with halides or sulfonates by oxidative addition, generating reactive intermediates having the organic group attatched to Pd(II) by  -bond. The oxidative addition reaction is very useful for aryl and alkenyl halides, but the products form saturated alkyl halides usually decompose by elimination. The reactions involving organopalladium intermediates are done in the presence of phosphine ligands. These ligands coodinate at palladium and play a key role in the reaction by influencing the reactivity. Another general point concerns the relative weakness of the C-Pd bond and, especially, the instability of alkyl palladium species in which there is a  hydrogen.

Palladium-catalyzed Nucleophilic Substitution and Alkylation. Wacker reaction: catalytic method for conversion of ethylene to acetaldehyde. The first step is addition of water to the Pd-activated alkene. Enol The co-reagents CuCl 2 and O 2 serve to reoxidize the Pd(0) to Pd(II). The net reaction consumes only alkene and oxygen.

The Heck Reaction Heck Reaction: Aryl and alkenyl halides react with alkenes in the presence of catalytic amounts of palladium to give net substitution of the halide by the alkenyl group. The reaction is quite general and has been observed for simple alkenes, aryl sustituted alkenes, and electrophilic alkenes such as acrylic esters and N-vinylamides. The reactions are usually carried out in the presence of a phosphine ligand.

The reaction is initiated by oxidative addition of the halide to a palladium(0) species genreated in situ from the Pd(II) catalyst. The  -complex decomposes with regeneration of Pd(0) by  -elimination.

High halide concentration promotes formation of the anionic species [PdL 2 X] - by addition of a halide ligand. Use of trifluoromethanesulfonate anions promotes dissociation of the anion from the Pd(II) adduct and accelerates complexation with electron-rich alkene.

Aryl chlorides are not very reactive under normal Heck reaction conditions, but reaction can be achieved by inclusion of triphenylphosphonium salts with Pd(Oac) 2 or PdCl 2 as the catalyst. With vinyl ethers and N-vinylamides, it is possible to promote  arylation by use of bidentate phosphine ligands such as dppe and dppp, using aryl triflates as reactants. Electronic factors favor migration of the aryl group to the  carbon.

Allylic silanes show a pronounced tendency to react at the  carbon. This regiochemistry is attributed to the stabilization of cationic character at the  carbon by the silyl substituent Palladium-Catalyzed Cross Coupling Coupling with organometallic Reagents: cross-coupling reaction Organomagnesium, organozinc, mixed cuprate, stanne, or organoboron compounds The reaction is quite general for formation of sp2-sp2 and sp2-sp bonds in biaryls, dienes and polyenes and enyenes. There are also some conditions which can couple alkyl organometallic reagents, but these reactions are less general because of the tendency of alkylpalladium intermediates to decompose by  elimination

Pd-catalyzed cross-coupling of organometallic reagents

A promising development is the extension of Pd-catalyzed cross coupling to simple enolates and enolate equivalent, which provides an important way of arylating enolates which is normally a difficult transformation to accomplish. Use of tri-t-butylphsophine with a catalytic amount of Pd(OAc) 2 results in phenylation of the enolates of aromatic ketones and diethyl malonate. Arylation has also been observed with the diphosphine ligand, BINAP.

A combination of Pd(PPh 3 ) 4 and Cu(I) effects coupling of terminal alkynes with vinyl or aryl halides. The alkyne is presumably converted to the copper acetylide. The halide reacts with Pd(0) by oxidative addition. Transfer of the acetylide group to Pd results in reductive elimination and formation of the observed product. Sonogashira Coupling

Use of alkenyl halides in this reaction has proven to be an effective method for the synthesis of enynes. The reaction can be carried out directly with the alkyne, using amines for deprotonation Coupling with Stannes: Stille Coupling The approximate order of effectiveness of transfer of groups from tin is alkynyl>alkenyl>aryl>methyl>alkyl, so unsaturated groups are normally transferred selectively.

Subsequent studies have found improved ligands, including tri-2-furylphsophine and triphenylarsine. Aryl-aryl coupling rates are increased by the presence of Cu(I) co-catalyst. The reactions occur with retention of configuration at both the halide and the stanne. Very useful in stereospecific construction of dienes and polyenes. Tolerant to the various functional groups: ester, nitrile, nitro, cyano, and formyl groups

Masked form of formyl group Alkenyl triflates are also reactive

Coupling with Organoboranes: Suzuki couling Cross coupling in which the organometallic component is an aryl or vinyl boron compound: boronic acids, boronate esters, boranes. Transmetallation or oxidative addition can be the rate determining step

Suzuki Cross Coupling

Special case

In some synthetic applications, specific bases such as Cs 2 CO 3 or TlOH have been found preferable to NaOH. The reaction proceed with retention of double-bond configuration in both the boron derivative and the alkenyl halide.

Carbonylation Reactions

The detailed mechanism of such reactions have been shown to involve addition and elimination of phosphine.

These reactions can be carried out with stannes or boronic acids as the nucleophilic component.

Tandem carbonylation reaction

Monsanto Process (Acetic acid Synthesis): o c, 1-40 atm Ref: BASF process: cobalt-based high pressure process ( o C, atm)

8.3 Reactions Involving Organonickel Compounds Allylic halides react with nickel carbonyl, Ni(CO) 4 to give  -allyl complexes.

These reactions are believed to involve Ni(I) and Ni(III) intermediates in a chain process which is initiated by formation of a small amount of a Ni(I) sepcies.

This couplig reaction has been used intramolecularly to bring about cyclization of bis-allylic halides and was found useful in the preparation of large rings. Nickel carbonyl is an extremely toxic compound, and a number of other nickel reagents with generally similar reactivity can be used in its place.

Mediun sized ring can be formed in intramolecular reaction.

The key aspects of the mechanism are (1) the reductive elimination which occurs via a diaryl Ni(III) intermediates and (2) the oxidative addition which involves a Ni(I) species.

A soluble bis-phosphine complexes, Ni(dppe) 2 Cl 2, is a particularly effective catalyst. The main distinction between this reaction and Pd-catalyzed cross coupling is that the nickel reaction can be more readily applied to saturated alkyl groups because of a reduced tendency for  -elimination. The synthesis of cyclophane-type structures by use of dihaloarenes and Grignard reagents from  -dihalides.

When secondary Grignard reagents are used, the coupling product sometimes is derived from the corresponding primary alkyl group. This transformation can occur by reversible formation. Styrene serves to stabilize the active catalytic species, and among the styrene derivatives, m-trifluoromethylstyrene was the best.

The main advantage of nickel is that it reacts more readily with arylchlorides and methanesulfonates than does the Pd system. These reactants may be more economical than iodides or triflates in large-scale synthesis. Vinyl phosphates can be used, and these are in some cases more readily obtained and handled than vinyl triflates.

8.4 Reactions Involving Rhodium and Cobalt Hydroformylation The key steps in reaction are addition of hydridorhodium to the double bond of the alkene and migration of the alkyl group to the complexed carbon monoxide.

The acylrhodium intermediate is trapped by internal nucleophiles. Fischer-Tropsch Process: reductive conversion of carbon monoxide to alkane by reacting with hydrogen gas. Synthetic hydrocarbon fuels.( ) In1944, 600,000 ton/yr was produced. Since 1957 South Africa use this method, Sasol Process.

Under appropriate conditions, rhodium catalyst can be used for the decarbonylation of aldehyde and acyl chlorides.

The use of cobalt for synthetic purpose is quite limited. Vinyl bromides and idodides couple with Grignard reagents in good yields, but a good donor solvent such as NMP or DMPU is required as a cocatalyst.

8.5 Organometallic Compounds with  bonding Among the classes of organic compounds that serve as  ligands are alkene, allyl, dienes, cyclopentadiene anion, and aromatic compounds. a)The number of electrons that can be accommodated by the metal orbitals b)the oxidation level of the metal, c)the electron character of other ligands on the metal The reactivity depends on the following factors

Both thermal and photochemical reactions are used.  -allyl complexes of nickel can be prepared either by oxidative addition on Ni(0) or by transmetallation of a Ni(II) salt.

Oxidative decomposition Trapping experiments In 1956, Longuet and Orgel propose the complex compound. In 1959, Criegee isolated the complex.

One of the best known of the  -organometallic compounds is ferrocene. The molecules behave as an electron-rich aromatic system, and electrophilic substitution reactions occur readily. Reagents that are relatively strong oxidizing agents, such as the halogens, effect oxidation at iron and destroy the compound. Effective Atomic Number: 18

One of the most useful types of  -complexes of aromatic compounds from the synthetic point of view are chromium complexes obtained by heating benzene or other aromatics with Cr(CO) 6. The Cr(CO) 3 unit is strongly electron-withdrawing and activates the ring to nucleophilic attack.

oxidize Existing substituent groups such as CH 3, OCH 3, and + NMe 3 exert a directive effect, often resulting in a major amount of the meta substitution product.