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

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-03-20 DOI:10.1021/acs.joc.4c02283
Zhiqi Yang, Jiaxin Xing, Yingli Xu, Junjie Wang, Pengcheng Zhou
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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.

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烯醇乙酸酯和磺酰肼电化学合成β-酮砜
研究了一种新型的、环境友好的电化学合成β-酮砜的方法。该方法可以在温和的条件下,通过易得的磺酰肼与醋酸烯醇反应合成β-酮砜,尤其不需要过渡金属催化剂或氧化剂,收率高。系统地探讨了各种磺酰肼和烯醇乙酸酯的反应范围。利用电化学流动电池成功地完成了β-酮砜的规模化合成,证明了该方法的工业适用性。此外,通过自由基清除实验和循环伏安法研究了其潜在的反应机理。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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