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Trifluoromethylation of enamines under acidic conditions
Authors:Roman T. Gritsenko  Pavel A. Belyakov  Marina I. Struchkova  Vladimir A. Tartakovsky
Affiliation:N.D. Zelinsky Institute of Organic Chemistry, 119991 Moscow, Leninsky prosp. 47, Russia
Abstract:A method for the trifluoromethylation of enamines using Me3SiCF3 leading to α-CF3-substituted amines is described. The reaction is promoted by hydrofluoric acid generated from KHF2 and either trifluoroacetic or triflic acid, and involves protonation of the enamine followed by transfer of the CF3-carbanion from the silicon reagent to the cationic electrophile.
Keywords:Enamines   Iminium ions   Trifluoromethylation
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