Multicomponent Selective Thioetherification of KSAc: Easy Access to Symmetrical/Unsymmetrical 4‐Alkylthio‐3‐halo‐2(5H)‐furanones

Author:

Zhou Yong‐Jun1,Fang Yong‐Gan1,Yang Kai2,Yu Shi‐Wei1,Chen Zu‐Jia1,Wang Bi‐Cheng3,Zhan Hai‐Ying3,Wang Zhao‐Yang1ORCID

Affiliation:

1. School of Chemistry South China Normal University GDMPA Key Laboratory for Process Control and Quality Evaluation of Chiral Pharmaceuticals Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine Key Laboratory of Theoretical Chemistry of Environment Ministry of Education Guangzhou Guangdong 510006 P. R. China

2. College of pharmacy Gannan Medical University Ganzhou 341000 P. R. China

3. School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University Zhongshan P. R. China

Abstract

AbstractAn easy two‐/three‐component selective thioetherification of KSAc for the synthesis of a series of symmetrical/unsymmetrical 4‐alkylthio‐3‐halo‐2(5H)‐furanones has been described. The reaction without any metal catalyst or additive is carried out in air atmosphere at room temperature for 5 h, only using potassium thioacetate as an odourless sulfur source and a base simultaneously. The broad substrate scope and high yield make it important for the studies on both constructing C−S bond based on non‐aryl Csp2−X bond and synthesizing new 2(5H)‐furanone functional molecules.

Funder

Basic and Applied Basic Research Foundation of Guangdong Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry

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