Issue 42, 2021

1,2-Bis-perfluoroalkylations of alkenes and alkynes with perfluorocarboxylic anhydrides via the formation of perfluoroalkylcopper intermediates

Abstract

A novel, Cu-mediated protocol toward the 1,2-bis-perfluoroalkyaltion of alkenes/alkynes was developed. The method proceeded with perfluorocarboxylic anhydrides as inexpensive and readily available perfluoroalkyl sources. Diacyl peroxide was generated in situ from the perfluorocarboxylic anhydrides and H2O2. The key step in this reaction is the formation of a stable perfluoroalkylcopper intermediate that is achieved with the aid of a bipyridyl ligand. Subsequent reaction of the intermediate with perfluoroalkyl-containing alkyl or vinyl radicals affords the desired products.

Graphical abstract: 1,2-Bis-perfluoroalkylations of alkenes and alkynes with perfluorocarboxylic anhydrides via the formation of perfluoroalkylcopper intermediates

Supplementary files

Article information

Article type
Communication
Submitted
04 Aug 2021
Accepted
28 Aug 2021
First published
15 Sep 2021
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2021,19, 9148-9153

1,2-Bis-perfluoroalkylations of alkenes and alkynes with perfluorocarboxylic anhydrides via the formation of perfluoroalkylcopper intermediates

T. Tagami, Y. Aoki, S. Kawamura and M. Sodeoka, Org. Biomol. Chem., 2021, 19, 9148 DOI: 10.1039/D1OB01529J

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