Electrochemical debrominative hydrogenation/deuteration of 2-bromo-<i>N</i>-arylacetamides

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

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc00530b
Citations
3
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
2.37
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article

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

Maya Shankar Singh, Malkeet Singh, Saurabh Singh, Ashvani K. Singh
3 citations
Chemical Communications
Chemical Reactions and Isotopes
2.37
article

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

Maya Shankar Singh, Malkeet Singh, Saurabh Singh, Ashvani K. Singh
article en
3 citations

Abstract

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

Chemical CommunicationsVol. 61(35)
Banaras Hindu University (IN)
Openalex Percentile: Top 13%
Chemical Reactions and Isotopes
2.37
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