Cathodic C-H Trifluoromethylation of Arenes and Heteroarenes Enabled by an in Situ-Generated Triflyltriethylammonium Complex.

08:00 EDT 12th September 2019 | BioPortfolio

Summary of "Cathodic C-H Trifluoromethylation of Arenes and Heteroarenes Enabled by an in Situ-Generated Triflyltriethylammonium Complex."

While several trifluoromethylation reactions involving the electrochemical generation of CF radicals via anodic oxidation have been reported, the alternative cathodic, reductive radical generation has remained elusive. Herein, the first cathodic trifluoromethylation of arenes and heteroarenes is reported. The method is based on the electrochemical reduction of an unstable triflyltriethylammonium complex generated in situ from inexpensive triflyl chloride and triethylamine, which produces CF radicals that are trapped by the arenes on the cathode surface.


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This article was published in the following journal.

Name: Organic letters
ISSN: 1523-7052


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