有机化学 ›› 2014, Vol. 34 ›› Issue (1): 190-196.DOI: 10.6023/cjoc201307026 上一篇    下一篇

研究论文

溴化二甲基溴化硫催化下合成N-取代吡咯类化合物

岳闽敏, 刘巨艳, 王英, 袁斌   

  1. 天津师范大学化学学院 天津市功能分子结构与性能重点实验室 无机-有机杂化功能材料化学省部共建教育部重点实验室 天津 300387
  • 收稿日期:2013-07-17 修回日期:2013-09-02 发布日期:2013-09-06
  • 通讯作者: 刘巨艳,王英 E-mail:hxxyljy@mail.tjnu.edu.cn
  • 基金资助:

    天津市自然科学基金(Nos. 12JCZDJC34300,11JCYBJC03600);青年科学基金(No. 21001080)资助项目.

Synthesis of N-Substituted Pyrroles Catalyzed by Bromodimethylsulfonium Bromide

Yue Minmin, Liu Juyan, Wang Ying, Yuan Bin   

  1. Tianjin Key Laboratory of Structure and Performance for Functional Molecule, Key Laboratory of Inorganic-Organic Hybrid Functional Material Chemistry, Ministry of Education, College of Chemistry, Tianjin Normal University, Tianjin 300387
  • Received:2013-07-17 Revised:2013-09-02 Published:2013-09-06
  • Supported by:

    Project supported by the Natural Science Foundation of Tianjin City (Nos. 12JCZDJC34300, 11JCYBJC03600), the Young Scientist Fund (No. 21001080).

室温、无溶剂条件下,以溴化二甲基溴化硫(BDMS)为催化剂,以2,5-己二酮和伯胺类化合物为原料,能高收率的实现一系列N-取代吡咯衍生物的合成. 所有化合物结构通过1H NMR,13C NMR和元素分析确定.

关键词: 吡咯, 溴化二甲基溴化硫(BDMS), 合成

A series N-substituted pyrroles were prepared efficiently in high yields by the condensation of 2,5-hexanedione with primary amines in the presence of bromodimethylsulfonium bromide (BDMS) at room temperature under solvent-free conditions. All products were characterized by 1H NMR, 13C NMR spectra and elemental analysis.

Key words: pyrroles, bromodimethylsulfonium bromide (BDMS), synthesis