Issue 35, 2025

Electrochemical debrominative hydrogenation/deuteration of 2-bromo-N-arylacetamides

Abstract

Herein, we report a facile and efficient electro-reductive debrominative hydrogenation/deuteration of 2-bromo-N-aryl acetamides using H2O/D2O as an economical source of hydrogen/deuterium at room temperature. The reactions proceeded efficiently via C–Br bond activation, enabling facile synthesis of a range of N-substituted amides in moderate to high yields with broad functional group compatibility.

Graphical abstract: Electrochemical debrominative hydrogenation/deuteration of 2-bromo-N-arylacetamides

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2025
Accepted
26 Mar 2025
First published
27 Mar 2025

Chem. Commun., 2025,61, 6478-6481

Electrochemical debrominative hydrogenation/deuteration of 2-bromo-N-arylacetamides

S. Singh, M. Singh, A. Singh and M. S. Singh, Chem. Commun., 2025, 61, 6478 DOI: 10.1039/D5CC00530B

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