Electrochemical Synthesis of β-Keto Sulfones from Enol Acetates and Sulfonyl Hydrazides

A novel and environmentally friendly strategy has been developed for the efficient electrochemical synthesis of β-keto sulfones. This method enables the synthesis of β-keto sulfones by reacting easily available sulfonylhydrazide with enol acetate under mild conditions, especially without the need for transition metal catalysts or oxidants, which can achieve high yields. The scope of this reaction was systematically explored with various sulfonyl hydrazides and enol acetates. The scale-up synthesis of β-keto sulfones was successfully accomplished using an electrochemical flow cell, demonstrating the industrial applicability of this approach. Moreover, the underlying reaction mechanism was further investigated through free radical scavenging experiments and cyclic voltammetry studies.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-03-20
DOI
https://doi.org/10.1021/acs.joc.4c02283
Citations
3
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
2.81

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article

Electrochemical Synthesis of β-Keto Sulfones from Enol Acetates and Sulfonyl Hydrazides

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3 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
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article

Electrochemical Synthesis of β-Keto Sulfones from Enol Acetates and Sulfonyl Hydrazides

Pengcheng Zhou, Zhiqi Yang, Yingli Xu, Jun‐Jie Wang, Jiaxin Xing
article en
3 citations

Abstract

A novel and environmentally friendly strategy has been developed for the efficient electrochemical synthesis of β-keto sulfones. This method enables the synthesis of β-keto sulfones by reacting easily available sulfonylhydrazide with enol acetate under mild conditions, especially without the need for transition metal catalysts or oxidants, which can achieve high yields. The scope of this reaction was systematically explored with various sulfonyl hydrazides and enol acetates. The scale-up synthesis of β-keto sulfones was successfully accomplished using an electrochemical flow cell, demonstrating the industrial applicability of this approach. Moreover, the underlying reaction mechanism was further investigated through free radical scavenging experiments and cyclic voltammetry studies.

The Journal of Organic ChemistryVol. 90(13)
Wuhan Textile University (CN)
Hubei Provincial Department of Education
Clean water and sanitation
Openalex Percentile: Top 11%
Sulfur-Based Synthesis Techniques
2.81
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