Issue 79, 2016, Issue in Progress

Trifluoromethylation of (hetero)aryl iodides and bromides with copper(i) chlorodifluoroacetate complexes

Abstract

A new copper-mediated trifluoromethylation reaction using copper(I) chlorodifluoroacetate complexes as reagents is reported. The complex [L2Cu][O2CCF2Cl] (L = bpy, dmbpy, phen) reacted with (hetero)aryl iodides and bromides in the presence of CsF in DMF at 75 °C to afford the trifluoromethylarenes in good to excellent yields. High compatibility with various chemical functions or (hetero)cycles was also observed in the reaction. A reaction mechanism involving a difluorocarbene intermediate, along with a subsequent formation of a –CF3 anion was proposed.

Graphical abstract: Trifluoromethylation of (hetero)aryl iodides and bromides with copper(i) chlorodifluoroacetate complexes

Supplementary files

Article information

Article type
Paper
Submitted
15 Jun 2016
Accepted
02 Aug 2016
First published
02 Aug 2016

RSC Adv., 2016,6, 75465-75469

Trifluoromethylation of (hetero)aryl iodides and bromides with copper(I) chlorodifluoroacetate complexes

X. Lin, Z. Li, X. Han and Z. Weng, RSC Adv., 2016, 6, 75465 DOI: 10.1039/C6RA15547B

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