有机化学 ›› 2017, Vol. 37 ›› Issue (6): 1556-1559.DOI: 10.6023/cjoc201612003 上一篇    下一篇

研究简报

室温下叔丁醇钾促进烷基芳基硫醚的合成与机理研究(英文)

郭芳杰, 何雨轩, 王景芸, 孙京, 周明东   

  1. 辽宁石油化工大学化学与材料科学学院 抚顺 113001
  • 收稿日期:2016-12-02 修回日期:2017-01-14 发布日期:2017-02-17
  • 通讯作者: 孙京,周明东 E-mail:sunjing@lnpu.edu.cn,mingdong.zhou@lnpu.edu.cn
  • 基金资助:

    国家自然科学基金(No.21101085)、辽宁省自然科学基金(No.2015020196)、抚顺市科技厅(No.FSKJHT201423)、辽宁省高等学校优秀人才支持计划(No.LJQ2012031)、辽宁石油化工大学引进人才科研启动基金(No.2016XJJ-006)资助项目.

Potassium tert-Butoxide Promoted Formation of Alkyl Aryl Thioethers at Room Temperature: Synthesis and Mechanism

Guo Fangjie, He Yuxuan, Wang Jingyun, Sun Jing, Zhou Mingdong   

  1. School of Chemistry and Materials Science, Liaoning Shihua University, Fushun 113001
  • Received:2016-12-02 Revised:2017-01-14 Published:2017-02-17
  • Contact: 10.6023/cjoc201612003 E-mail:sunjing@lnpu.edu.cn,mingdong.zhou@lnpu.edu.cn
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21101085), the Natural Science Foundation of Liaoning Province (No. 2015020196), the Fushun Science & Technology Program (No. FSKJHT 201423), the Liaoning Excellent Talents Program in University (No. LJQ2012031), and the Talent Scientific Research Fund of Liaoning Shihua University (No. 2016XJJ-006).

研究了在无金属参与条件下芳基溴化物与烷基硫醇的C—S交叉偶联反应.研究表明在室温、KOtBu强碱作用条件下,各种缺电子的芳基溴化物与烷基硫醇均可以顺利地发生C—S交叉偶联反应,高产率地得到了一系列烷基芳基硫醚类产物.本研究同时对非金属参与的偶联反应机理进行了探讨.

关键词: C—S交叉偶联, 芳基溴化物, 机理, 烷基芳基硫醚

The C—S cross-coupling of aryl halides with alkyl thiols under transition metal-free conditions was investigated. Good to excellent yields can be obtained for a variety of electron-poor aryl halides with alkyl thiols in the presence of KOtBu even at room temperature. The mechanisms for transition metal-free coupling reactions are discussed.

Key words: C—S cross-coupling, aryl halides, mechanism, alkyl aryl thioethers