Electroreductive amination of carboxylic acids by cobalt catalysis

Catalytic reduction of carboxylic acids to valuable chemicals is highly desirable yet challenging for both biomass conversion and organic synthesis. Here we describe an efficient and sustainable electrocatalytic hydrogenation of carboxylic acids with amines utilizing protons as the hydrogen source. The application of an earth-abundant cobalt complex enables electrochemical generation of a cobalt-hydride intermediate, which serves as the key catalytically active species for this reductive process. Obviating the need for flammable H<sub>2</sub> gas or sensitive hydrides, this general hydrogenative coupling of carboxylic acids with amines and nitroarenes allows producing a wide range of structurally diverse complex alkylamines under mild electrocatalytic conditions. Furthermore, the practicality and versatility of this protocol are demonstrated through its application in valuable isotope labeling using readily available deuterium sources.

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Publication Details

Journal
Nature Communications
Published
2025-08-04
DOI
https://doi.org/10.1038/s41467-025-62396-4
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.07

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article

Electroreductive amination of carboxylic acids by cobalt catalysis

Zhizheng Chen, Shuanglin Qu, Huihua Bi, Jie Liu et al.
2 citations
Nature Communications
Asymmetric Hydrogenation and Catalysis
1.07
article

Electroreductive amination of carboxylic acids by cobalt catalysis

Zhizheng Chen, Shuanglin Qu, Huihua Bi, Jie Liu, Chong−Wen Bi
article en
2 citations

Abstract

Catalytic reduction of carboxylic acids to valuable chemicals is highly desirable yet challenging for both biomass conversion and organic synthesis. Here we describe an efficient and sustainable electrocatalytic hydrogenation of carboxylic acids with amines utilizing protons as the hydrogen source. The application of an earth-abundant cobalt complex enables electrochemical generation of a cobalt-hydride intermediate, which serves as the key catalytically active species for this reductive process. Obviating the need for flammable H<sub>2</sub> gas or sensitive hydrides, this general hydrogenative coupling of carboxylic acids with amines and nitroarenes allows producing a wide range of structurally diverse complex alkylamines under mild electrocatalytic conditions. Furthermore, the practicality and versatility of this protocol are demonstrated through its application in valuable isotope labeling using readily available deuterium sources.

Nature CommunicationsVol. 16(1)
Hunan University (CN), Bay Institute (US)
National Natural Science Foundation of China, Hunan University, Fundamental Research Funds for the Central Universities
Responsible consumption and production
Openalex Percentile: Top 22%
Asymmetric Hydrogenation and Catalysis
1.07
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Electroreductive amination of carboxylic acids by cobalt catalysis — Zhizheng Chen, Shuanglin Qu, et al. · Nature Communications (2025) | TGRS Research Map | TGRS