Issue 12, 2011

Protolytic defluorination of trifluoromethyl-substituted arenes

Abstract

A series of trifluoromethyl-substituted arenes were studied in their reactions with Brønsted superacids. The products from these reactions suggest the formation of reactive electrophiles, such as carbocations, acylium cations or equivalent electrophilic species. As such, Friedel–Crafts-type reactions occur between these species and arene nucleophiles. NMR studies were done, and the results suggest the formation of an acyl group from the trifluoromethyl groups in the superacid.

Graphical abstract: Protolytic defluorination of trifluoromethyl-substituted arenes

Supplementary files

Article information

Article type
Paper
Submitted
30 Dec 2010
Accepted
07 Apr 2011
First published
06 May 2011

Org. Biomol. Chem., 2011,9, 4545-4549

Protolytic defluorination of trifluoromethyl-substituted arenes

A. Kethe, A. F. Tracy and D. A. Klumpp, Org. Biomol. Chem., 2011, 9, 4545 DOI: 10.1039/C0OB01276A

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