Cathode–Anode Synergy Electrosynthesis of Propanamide via a Bipolar C–N Coupling Reaction

Propanamide is a crucial synthetic intermediate in pharmaceuticals for the preparation of antibacterial and anticancer drugs. Conventional synthesis of propanamide involves the reaction of carboxylic acid derivatives with amines, which requires harsh reaction conditions, leading to an unfavorable environmental footprint. Here, we present a cathode-anode synergistic electrochemical strategy to transform nitrate and n-propanol into propanamide under ambient conditions, where both the cathode catalyst Co<sub>3</sub>O<sub>4</sub>/SiC and the anode catalyst Ti contribute distinctively to the electrochemical process. The CH<sub>3</sub>CH<sub>2</sub>CHO produced at the Ti anode can diffuse and react with the adsorbed intermediate *NH<sub>2</sub>OH on the surface of the cathode catalyst to form propanamide. The synergistic reactions at both electrodes collectively enhance the efficiency of the propanamide synthesis. This design enables efficient propanamide production in a flow cell at the gram scale with a remarkable yield of 986.13 μmol/(cm<sup>2</sup>·h) at current densities of up to 650 mA/cm<sup>2</sup>. Our reports present a new option for environmentally friendly C-N bond synthesis, and the insights can be useful for the electrosynthesis of a wider scope of amides.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2025-05-02
DOI
https://doi.org/10.1021/jacs.5c01744
Citations
12
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
4.67

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cathode–Anode Synergy Electrosynthesis of Propanamide via a Bipolar C–N Coupling Reaction

Jin Liu, An‐Hui Lu, Ming‐Hao Guan, Xiao Zhou et al.
12 citations
Journal of the American Chemical Society
Ammonia Synthesis and Nitrogen Reduction
4.67
article

Cathode–Anode Synergy Electrosynthesis of Propanamide via a Bipolar C–N Coupling Reaction

Jin Liu, An‐Hui Lu, Ming‐Hao Guan, Xiao Zhou, Haonan Xu, Tao Wu
article en
12 citations

Abstract

Propanamide is a crucial synthetic intermediate in pharmaceuticals for the preparation of antibacterial and anticancer drugs. Conventional synthesis of propanamide involves the reaction of carboxylic acid derivatives with amines, which requires harsh reaction conditions, leading to an unfavorable environmental footprint. Here, we present a cathode-anode synergistic electrochemical strategy to transform nitrate and n-propanol into propanamide under ambient conditions, where both the cathode catalyst Co<sub>3</sub>O<sub>4</sub>/SiC and the anode catalyst Ti contribute distinctively to the electrochemical process. The CH<sub>3</sub>CH<sub>2</sub>CHO produced at the Ti anode can diffuse and react with the adsorbed intermediate *NH<sub>2</sub>OH on the surface of the cathode catalyst to form propanamide. The synergistic reactions at both electrodes collectively enhance the efficiency of the propanamide synthesis. This design enables efficient propanamide production in a flow cell at the gram scale with a remarkable yield of 986.13 μmol/(cm<sup>2</sup>·h) at current densities of up to 650 mA/cm<sup>2</sup>. Our reports present a new option for environmentally friendly C-N bond synthesis, and the insights can be useful for the electrosynthesis of a wider scope of amides.

Journal of the American Chemical SocietyVol. 147(19)
Dalian University of Technology (CN)
Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 4%
Ammonia Synthesis and Nitrogen Reduction
4.67
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.