有机化学 ›› 2008, Vol. 28 ›› Issue (10): 1740-1743. 上一篇    下一篇

研究论文

一水硫酸氢钠无溶剂催化合成4-甲基香豆素

杨金会*; 计从斌; 赵艳敏   

  1. (宁夏大学能源化工重点实验室 银川 750021)
  • 收稿日期:2008-01-17 修回日期:2008-04-08 发布日期:2008-10-20
  • 通讯作者: 杨金会

NaHSO4•H2O Catalyzed Synthesis of Coumarin Derivatives under Solvent-Free Conditions

YANG, Jin-Hui*; JI, Cong-Bin; ZHAO, Yan-Min

  

  1. (Key Laboratory of Energy Resources & Chemical Engineering, Ningxia Universty, Yinchuan 750021)
  • Received:2008-01-17 Revised:2008-04-08 Published:2008-10-20
  • Contact: YANG, Jin-Hui

NaHSO4•H2O(摩尔分数为0.1)催化下, 取代酚与乙酰乙酸乙酯(物质的量比1∶1.2)在无溶剂条件下, 通过Pechmann缩合反应, 合成了9个4-甲基香豆素衍生物, 反应时间3~5 h, 产率23%~91%, 反应条件温和、操作简便有效. 研究结果表明, 当苯酚环上取代基为一个羟基或氨基能显著加速反应, 提高产率, 苯环上更多的取代基则对反应没有促进作用; 当苯酚环上取代基为吸电子基团时, 则不发生反应或者产率很低.

关键词: 香豆素, 无溶剂反应, Pechmann反应, H2O, NaHSO4•

Nine 4-methylcoumarin derivatives were synthesized from phenols and ethyl acetoaceate at a molar ratio of 1∶1.2 via Pechmann condensation using NaHSO4•H2O (10 mol%) as catalyst under solvent-free conditions. The method was simple, green and efficient, and the reaction time was ranged from 3 to 5 h with the yields from 23% to 91%. The effects of substitution groups in the different positions of the aromatic ring on the reaction were investigated. The results showed that the activation group substituted on phenols, such as hydroxyl group or amino group, was favorable to the condensation reaction, but one more substitution group on the aromatic ring was less favorable to the reaction, the electron-withdrawing group substituted on phenols, such as nitro-group, led to no reaction or poor yields.

Key words: Pechmann condensation, coumarin, NaHSO4•, solvent-free reaction, H2O