4.8 Article

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

Journal

ORGANIC LETTERS
Volume 21, Issue 19, Pages 7970-7975

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02948

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Funding

  1. Austrian COMET Program by the Austrian Federal Ministry of Transport, Innovation and Technology (BMVIT) [862766]
  2. Austrian COMET Program by the Austrian Federal Ministry of Science, Research and Economy (BMWFW) [862766]
  3. Austrian COMET Program by the State of Styria (Styrian Funding Agency SFG) [862766]

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While several trifluoromethylation reactions involving the electrochemical generation of CF3 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 CF3 radicals that are trapped by the arenes on the cathode surface.

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