Add time:08/03/2019         Source:sciencedirect.com

A mild and efficient trifluoromethylselenolation of acid chlorides with [(bpy)Cu(SeCF3)]2 (1) in the presence of a catalytic amount of metallic iron powder is described. Easily available benzoyl chloride derivatives and alkyl acid chlorides are smoothly converted into the corresponding Se-trifluoromethyl esters in good to excellent yields. This simple transformation demonstrates a broad substrate scope with respect to acid chlorides, and is amenable to being carried out on gram scales.

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