Issue 91, 2015

Electroorganic synthesis of nitriles via a halogen-free domino oxidation–reduction sequence

Abstract

A direct electroorganic sequence yielding nitriles from oximes in undivided cells is reported. Despite the fact that intermediate nitrile oxides might be formed, the method is viable to prepare benzonitriles without substituents ortho to the aldoxime moiety. This constant current method is easy to perform for a broad scope of substrates and employs common electrodes, such as graphite and lead.

Graphical abstract: Electroorganic synthesis of nitriles via a halogen-free domino oxidation–reduction sequence

Supplementary files

Article information

Article type
Communication
Submitted
31 Jul 2015
Accepted
17 Sep 2015
First published
17 Sep 2015
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 16346-16348

Author version available

Electroorganic synthesis of nitriles via a halogen-free domino oxidation–reduction sequence

M. F. Hartmer and S. R. Waldvogel, Chem. Commun., 2015, 51, 16346 DOI: 10.1039/C5CC06437F

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