SIOC English
有机化学
高级检索

有机化学 ›› 2006, Vol. 26 ›› Issue (02): 239-241. 上一篇    下一篇

研究简报

4-溴-2-环戊烯砜酯化衍生物的合成

霍延平1,2,3，曾和平*,2，江焕峰1,2   

  1. (1中国科学院广州化学研究所 广州510650)
    (2华南理工大学化学科学学院 广州 510641)
    (3中国科学院研究生院 北京 100039)
  • 收稿日期:2005-04-26 修回日期:2005-08-18 发布日期:2006-01-21
  • 通讯作者: 曾和平

Synthesis of 4-Bromo-2-sulfolene Ester Derivatives

HUO Yan-Ping1,2,3,ZENG He-Ping*,2,JIANG Huan-Feng1,2   

  1. (1 Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou 510650)
    (2 School of Chemistry, South China University of Technology, Guangzhou 510641)
    (3 Graduate University of Chinese Academy of Sciences, Beijing 100039)
  • Received:2005-04-26 Revised:2005-08-18 Published:2006-01-21
  • Contact: ZENG He-Ping

PDF

1609

被引次数

4

以3,4-二溴环戊砜(1)为原料, 在无水吡啶作用下发生消除反应, 得到反应中间体4-溴-2-环戊烯砜(2), 再分别与一系列取代苯甲酸盐3a～3c以及茜素黄GG (3d)发生酯化反应, 合成出4种新环戊烯砜衍生物4a～4d, 并用IR, 1H NMR, MS, 元素分析等表征了它们的结构.

关键词: 3, 4-二溴环戊砜, 酯化反应, 4-溴-2-环戊烯砜, 取代苯甲酸盐, 茜素黄GG

3,4-Dibromosulfolane (1) was treated with pyridine to form 4-bromo-2-sulfolene (2) by elimination reaction. 4-Bromo-2-sulfolene (2) reacted with substituted benzoic acid salts 3a～3c or alizarin yellow (3d) to give four novel allylic substitution products 4a～4d by esterification reaction, respectively. These novel compounds 4a～4d were determined by IR, 1H NMR, MS spectra and elemental analysis.

Key words: substituted benzoic acid salt, alizarin yellow, esterification, 4-bromo-2-sulfolene, 3,4-dibromosulfolane