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(S)-(-)-4-[反式-4’-(反式-4”-丙基环己基)-环己基]-1-(1-甲基庚氧基)-2,6-二氟苯的合成
引用本文:李辉,杜渭松,李建.(S)-(-)-4-[反式-4’-(反式-4”-丙基环己基)-环己基]-1-(1-甲基庚氧基)-2,6-二氟苯的合成[J].应用化工,2009,38(5).
作者姓名:李辉  杜渭松  李建
作者单位:西安近代化学研究所,光电材料事业部,陕西,西安,710065
摘    要:报道了手性添加剂(S)-(-)-4-反式-4’-(反式-4"-丙基环己基)-环己基]-1-(1-甲基庚氧基)-2,6-二氟苯的合成方法,通过格氏偶联、硫酸氢钾催化脱水、催化氢化、顺反异构化、超低温反应、双氧水氧化、M itsunobu成醚反应共7步反应合成了目标产物,总收率21%。经IR、MS、1H NMR鉴定,结构正确,并测定了其扭曲力。

关 键 词:手性添加剂  合成  异构化  扭曲力

Synthesis of (S)-(-)-4-[trans-4'-(trans-4"-propylcyclohexyl)-cyclohexyl]-1-(1-methylheptyloxy)-2,6-difluorbenzol
LI Hui,DU Wei-song,LI Jian.Synthesis of (S)-(-)-4-[trans-4'-(trans-4"-propylcyclohexyl)-cyclohexyl]-1-(1-methylheptyloxy)-2,6-difluorbenzol[J].Applied chemical industry,2009,38(5).
Authors:LI Hui  DU Wei-song  LI Jian
Abstract:The synthetic method of(S)-(-)-4-trans-4'-(trans-4"-propylcyclohexyl)-cyclohexyl]-1-(1-methylheptyloxy)-2,6-difluorbenzol is reported.The target compound was synthesized through seven steps reactions include grignard coupling,dehydration,hydrogenation,isomerization,ultra low temperature reaction,oxidation and Mitsunobu etherification.The total yield is 21%.Structure identification was performed by IR,MS,1H NMR.The helix twisting power is measured.
Keywords:chiral dopants  synthesis  isomerization  helix twisting power
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