5-羧戊基三苯基溴化膦的合成
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

R914.5;O622.5

基金项目:


Synthesis of (5-Carboxypentyl)triphenyphosphonium Bromide
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    5-羧戊基三苯基溴化膦广泛用于立体选择性药物的合成。由ε-己内酯和氢溴酸在H2SO4作用下,生成6-溴己酸,再与三苯基膦在甲苯溶剂中缩合生成5-羧戊基三苯基溴化膦(C24H26BrO2P)。通过实验考察了影响5-羧戊基三苯基溴化膦合成的各项因素。结果表明,当n(ε-己内酯)∶n(三苯基膦)∶n(氢溴酸)=1.0∶0.95∶1.4、回流反应温度、反应时间为14h,以ε-己内酯计的5-羧戊基三苯基溴化膦收率可达82.2%,经HPLC测定其纯度为98.3%。

    Abstract:

    The ylide (5-carboxypentyl)triphenyphosphonium bromide, which was widely used in the synthesie of stereo selectivity drug. 6-Bromohexanoic was synthesized withε-caprolaetone and hydrobromic acid over sulfuric acid, was synthesized via condensation with triphenylphosphine to produce (5-carboxypentyl)triphenyphosphonium bromide. The effect of reaction conditions on the properties of (5-carboxypentyl)triphenyphosphonium was investigated by method of experiments. The results show that the yield of (5-carboxypentyl)triphenyphosphonium could reach 82.2% and its content was 98.3% calculated by acetylacetone under the following reaction conditions: the molar ratio of ε-caprolaetone to triphenylphosphine and hydrobromic acid was 1.0∶0.95∶1.4, at reflux temperature, and the reaction time was 14 hours.

    参考文献
    相似文献
    引证文献
引用本文

杨明庆,张舰,马凌,魏忠林.5-羧戊基三苯基溴化膦的合成[J].精细化工,2012,29(4):0

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2011-10-24
  • 最后修改日期:2011-12-15
  • 录用日期:2011-12-16
  • 在线发布日期: 2012-03-20
  • 出版日期:
文章二维码