Reactions of organocopper reagents involve species containing copper-carbon bonds acting as nucleophiles in the presence of organic electrophiles. Organocopper reagents are now commonly used in organic synthesis as mild, selective nucleophiles for substitution and conjugate addition reactions. Since the discovery that copper(I) halides catalyze the conjugate addition of Grignard reagents in 1941, organocopper reagents have emerged as weakly basic, nucleophilic reagents for substitution and addition reactions. The constitution of organocopper compounds depends on their method of preparation and the various kinds of organocopper reagents exhibit different reactivity profiles. As a result, the scope of reactions involving organocopper reagents is extremely broad.
Organocopper complexes (RCu) are produced when a copper(I) halide and organolithium are combined. In conjunction with Lewis acidic additives such as boron trifluoride etherate, these reagents are used for conjugate addition reactions. Lower-order cuprates (R2CuLi, also known as Gilman reagents) result when organocopper complexes are treated with an equivalent of organolithium. Alternatively, they may be formed by the treatment of a copper(I) halide with two equivalents of organolithium. They undergo substitution, conjugate addition, and carbocupration reactions in the presence of the appropriate organic substrates. Mixed Gilman reagents consist of two different R groups, one of which is typically a non-transferable "dummy" group. Lower-order cyanocuprates (RCu(CN)Li) are similarly derived from an organolithium compound and copper(I) cyanide; however, intermediate organocopper complexes do not form during this reaction and thus only a single equivalent of organolithium reagent is necessary. Cyanocuprates undergo SN2' substitution in the presence of allyl electrophiles and conjugate addition reactions in the presence of enones. Higher-order cyanocuprates (R2Cu(CN)Li2) are formed upon the reaction of two equivalents of organolithium with copper(I) cyanide. These reagents are more reactive towards substitution than the corresponding lower-order cyanocuprates.
Mechanism and Stereochemistry
Substitution Reactions The mechanism of nucleophilic substitution by lower-order organocuprates depends in a profound way on the structure of the substrate, organocuprate, and reaction conditions. Early evidence suggested that a direct SN2 displacement was occurring; however more recent results suggest that invertive oxidative addition of copper(I) into the carbon-leaving group bond takes place, generating a copper(III) intermediate which then undergoes reductive elimination to generate the coupled product. Both of these mechanisms predict inversion at the electrophilic carbon, which is observed in a number of cases. On the other hand, experiments with radical traps and the observation of racemization during substitution suggest a radical mechanism.
(1)
Conjugate Addition Reactions In 1941, Kharash discovered that Grignard reagents add to cyclohexenone in presence of Cu(I) resulting in 1,4-addition instead of 1,2-addition. This work foreshadowed extensive studies on the conjugate additions to enones with organocuprates. Note that if a Grignard reagent (such as RMgBr) is used, the reaction with an enone would instead proceed through a 1,2-addition. The 1,4-addition mechanism of cuprates to enones goes through the nucleophilic addition of the Cu(I) species at the beta-carbon of the alkene to form a Cu(III) intermediate, followed by reductive elimination of Cu(I). In the original paper describing this reaction, methylmagnesium bromide is reacted with isophorone with and without 1 mole percent of added copper(I) chloride (see figure).
Without added salt the main products are alcohol B (42%) from nucleophilic addition to the carbonyl group and diene C (48%) as its dehydration reaction product. With added salt the main product is 1,4-adduct A (82%) with some C (7%). A 1,6-addition is also possible, for example in one step of the commercial-scale production of fulvestrant:
Enantioselective Variants Diastereoselective conjugate addition reactions of chiral organocuprates provide β-functionalized ketones in high yield and diastereoselectivity. A disadvantage of these reactions is the requirement of a full equivalent of enantiopure starting material.
(3) More recently, catalytic enantioselective methods have been developed based on the copper(I)-catalyzed conjugate addition of Grignard reactions to enones. The proposed mechanism involves transmetalation from the Grignard reagent to copper, conjugate addition, and rate-determining reductive elimination (see the analogous upper pathway in equation (2)).
(4)
Catalytic reactions Vinyl and aryl Grignard reagents couple with primary alkyl halides in the presence of a catalytic amount of a copper(I) halide salt. The use of Li2CuCl4 rather than simple copper(I) halide salts (CuX) improves yields of these coupling reactions.
(5) The addition of Grignard reagents to alkynes is facilitated by a catalytic amount of copper halide. Transmetalation to copper and carbocupration are followed by transmetalation of the product alkene back to magnesium. The addition is syn unless a coordinating group is nearby in the substrate, in which case the addition becomes anti and yields improve.
(6)
Stoichiometric reactions Propargyl methanesulfinates are useful substrates for the synthesis of allenes from stoichiometric organocopper complexes. In this case, the complexes were generated in situ through the combination of a Grignard reagent, copper(I) bromide, and lithium bromide. Organocopper complexes very often need Lewis acid activation in order to react efficiently; magnesium bromide generated in situ serves as an activating Lewis acid in this case.
(7) Alkenylcopper complexes, easily generated through carbocupration, are useful for the introduction of a vinyl group in the β position of a carbonyl compound. In this case, as above, magnesium bromide is serving as an activating Lewis acid.
(8) Epoxide opening with organocuprates is highly selective for the less hindered position. Substitution takes place with complete inversion of configuration at the electrophilic carbon.
(9) Generally, organocuprates react with allylic electrophiles in an anti SN2 fashion. In the reaction below, nearly complete inversion of configuration was observed despite the presence of a second stereocenter in the ring.
… excerpt ends here. Continue reading the full article.
