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The Corey–Fuchs reaction, also known as the Ramirez–Corey–Fuchs reaction, is a series of chemical reactions designed to transform an aldehyde into an alkyne. The formation of the 1,1-dibromoolefins via phosphine-dibromomethylenes was originally discovered by Desai, McKelvie and Ramirez. The second step of the reaction to convert dibromoolefins to alkynes is known as Fritsch–Buttenberg–Wiechell rearrangement. The overall combined transformation of an aldehyde to an alkyne by this method is named after its developers, American chemists Elias James Corey and Philip L. Fuchs. By suitable choice of base, it is often possible to stop the reaction at the 1-bromoalkyne, a useful functional group for further transformation. ==Reaction mechanism== The Corey–Fuchs reaction is based on a special case of the Wittig Reaction, where the phosphorus ylide is formed from dibromocarbene. This carbene is generated ''in situ'' from the reaction of Triphenylphosphine and carbon tetrabromide. Triphenylphosphine then attacks the nascent carbene to form the reactive ylide. This ylide undergoes a Wittig Reaction when exposed to an aldehyde. Deprotonation of the weakly acidic olefinic proton with butyllithium gives rise to a lithio-olefinic species which can undergo a beta-elimination to produce the bromoalkyne. Further treatment with butyllithium allows for a lithium–halogen exchange and the intermediate can be quenched with an electrophile, such as water or an alkyl halide, transforming the bromoalkyne to the terminal acetylene, or the internal alkyne, respectively. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Corey–Fuchs reaction」の詳細全文を読む スポンサード リンク
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