Issue 21, 2021

Difluorocarbene-based cyanodifluoromethylation of alkenes induced by a dual-functional Cu-catalyst

Abstract

Although cyanofluoroalkylation has received increasing attention, a toxic cyanation reagent is usually required. Herein, a Cu-catalyzed difluorocarbene-based cyanodifluoromethylation of alkenes with BrCF2CO2Et/NH4HCO3 under photocatalytic conditions is described. BrCF2CO2Et and NH4HCO3 serve as a carbon source and a nitrogen source of the nitrile group, respectively, avoiding the use of a stoichiometric toxic cyanation reagent. The Cu-complex plays a dual role. It is not only a photocatalyst, but also a coupling catalyst for the formation of a C–CN bond.

Graphical abstract: Difluorocarbene-based cyanodifluoromethylation of alkenes induced by a dual-functional Cu-catalyst

Supplementary files

Article information

Article type
Communication
Submitted
11 Jan 2021
Accepted
29 Jan 2021
First published
01 Feb 2021

Chem. Commun., 2021,57, 2649-2652

Difluorocarbene-based cyanodifluoromethylation of alkenes induced by a dual-functional Cu-catalyst

M. Zhang, J. Lin, C. Jin and J. Xiao, Chem. Commun., 2021, 57, 2649 DOI: 10.1039/D1CC00160D

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