Trifluoroacetone


Trifluoroacetone is an organofluorine compound with the chemical formula CF3CCH3. The compound is a colorless liquid with chloroform-like odour.

Preparation, reactions, uses

Trifluoroacetone is produced by decarboxylation of trifluoroacetoacetic acid:
The acetoacetic acid in turn is obtained via condensation of acetate and trifluoroacetate esters.
Trifluoroacetone has been examined as oxidizing agent in Oppenauer oxidation, in which case hydroxyl groups of secondary alcohols can be oxidized in the presence of hydroxy groups of primary alcohols.
Trifluoracetone is also used in a synthesis of 2-trifluoromethyl-7-azaindoles starting with 2,6-dihalopyridines. The derived chiral imine is used to prepare enantiopure α-trifluoromethyl alanines and diamines by a Strecker reaction followed by either nitrile hydrolysis or reduction.