Gilman reagent

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

A Gilman reagent is a lithium and copper (diorganocopper) reagent compound, R₂CuLi, where R is an organic radical. These are useful because they react with chlorides, bromides, and iodides to replace the halide group with an R group. This is extremely useful in creating larger molecules from smaller ones.

These reagents were discovered by Henry Gilman. Lithium dimethylcopper (CH₃)₂CuLi can be prepared by adding copper(I) iodide to methyl lithium in tetrahydrofuran at -78°C. In the reaction depicted in scheme 1 ^[1] the Gilman reagent is a methylating reagent reacting with an alkyne in an conjugate addition and the negative charge is trapped in a nucleophilic acyl substitution with the ester group forming a cyclic enone.

File:Gilman reaction example.png

See also[edit | edit source]

• Organolithium reagent
• Grignard reagent

External links[edit | edit source]

• National Pollutant Inventory - Copper and compounds fact sheet

References[edit | edit source]

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