Gilman reagent

A Gilman reagent is a lithium and copper (diorganocopper) reagent compound, R2CuLi, where R is an alkyl or aryl. These reagents are useful because, unlike related Grignard reagents and organolithium reagents, they react with organic halides to replace the halide group with an R group (the Corey–House reaction). Such displacement reactions allow for the synthesis of complex products from simple building blocks.[1]

Generalized chemical reaction showing Gilman reagent reacting with organic halide to form products and showing Cu(III) reaction intermediate
General structure of a Gilman reagent

Reactions

These reagents were discovered by Henry Gilman and coworkers.[2] Lithium dimethylcopper (CH3)2CuLi can be prepared by adding copper(I) iodide to methyllithium in tetrahydrofuran at −78 °C. In the reaction depicted below,[3] the Gilman reagent is a methylating reagent reacting with an alkyne in a conjugate addition, and the negative charge is trapped in a nucleophilic acyl substitution with the ester group forming a cyclic enone.

Scheme 1. Example Gilman reagent reaction

Due to the softness of the nucleophile, they do 1,4 addition on conjugated enones, rather than 1,2 addition.

Structure

Lithium dimethylcuprate exists as a dimer in diethyl ether forming an 8-membered ring. Similarly, lithium diphenylcuprate crystallizes as a dimeric etherate, [{Li(OEt2)}(CuPh2)]2.[4]

If the Li+ ions is complexed with the crown ether 12-crown-4, the resulting diorganylcuprate anions adopt a linear coordination geometry at copper.[5]

Mixed cuprates

More useful generally than the Gilman reagents are the so-called mixed cuprates with the formula [RCuX]− and [R2CuX]2−. Such compounds are often prepared by the addition of the organolithium reagent to copper(I) halides and cyanide. These mixed cuprates are more stable and more readily purified.[6] One problem addressed by mixed cuprates is the economical use of the alkyl group. Thus, in some applications, the mixed cuprate has the formula Li2[Cu(2-thienyl)(CN)R] is prepared by combining thienyllithium and cuprous cyanide followed by the organic group to be transferred. In this higher order mixed cuprate, both the cyanide and thienyl groups do not transfer, only the R group does.[7]

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See also

References
  1. J. F. Normant (1972). "Organocopper(I) Compounds and Organocuprates in Synthesis". Synthesis. 1972 (02): 63–80. doi:10.1055/s-1972-21833.
  2. Henry Gilman, Reuben G. Jones, and L. A. Woods (1952). "The Preparation of Methylcopper and some Observations on the Decomposition of Organocopper Compounds". Journal of Organic Chemistry. 17 (12): 1630–1634. doi:10.1021/jo50012a009.CS1 maint: multiple names: authors list (link)
  3. Modern Organocopper Chemistry, N. Krause Ed. Wiley-VCH, 2002.
  4. N. P. Lorenzen; E. Weiss (1990). "Synthesis and Structure of a Dimeric Lithium Diphenylcuprate:[{Li(OEt)2}(CuPh2)]2". Angew. Chem. Int. Ed. 29 (3): 300–302. doi:10.1002/anie.199003001.
  5. H. Hope; M. M. Olmstead; P. P. Power; J. Sandell; X. Xu (1985). "Isolation and x-ray crystal structures of the mononuclear cuprates [CuMe2]−, [CuPh2]−, and [Cu(Br)CH(SiMe3)2]−". J. Am. Chem. Soc. 107 (14): 4337–4338. doi:10.1021/ja00300a047.
  6. Steven H. Bertz, Edward H. Fairchild, Karl Dieter, "Copper(I) Cyanide" in Encyclopedia of Reagents for Organic Synthesis 2005, John Wiley & Sons. doi:10.1002/047084289X.rc224.pub2
  7. Bruce H. Lipshutz, Robert Moretti, Robert Crow "Mixed Higher-order Cyanocuprate-induced Epoxide Openings: 1-Benzyloxy-4-penten-2-ol" Org. Synth. 1990, volume 69, pp. 80. doi:10.15227/orgsyn.069.0080
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