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手性助剂樟脑磺酸酯的合成工艺研究
引用本文:刘秀娟,王歌云,厉连斌.手性助剂樟脑磺酸酯的合成工艺研究[J].化学世界,2012,53(5):300-302.
作者姓名:刘秀娟  王歌云  厉连斌
作者单位:江西教育学院理学分院,江西南昌,330029
基金项目:江西省教育厅科技计划项目(赣教科技便函字2002-01)
摘    要:以樟脑磺酸为起始原料,通过两步反应,合成了樟脑磺酸酯,并用IR和1 H NMR进行了表征。优化条件为:n(樟脑磺酰氯)∶n(甲醇)∶n(吡啶)=1.0∶2.5∶4.0,在-5℃下反应2h,樟脑磺酸甲酯的收率达到了73.2%,产品质量分数为99.6%。

关 键 词:樟脑磺酸甲酯  樟脑磺酸乙酯  樟脑磺酰氯  樟脑磺酸  手性助剂

Studies on Synthesis of Camphor Sulfonate as Chiral Auxiliary
LIU Xiu-juan , WANG Ge-yun , LI Lian-bin.Studies on Synthesis of Camphor Sulfonate as Chiral Auxiliary[J].Chemical World,2012,53(5):300-302.
Authors:LIU Xiu-juan  WANG Ge-yun  LI Lian-bin
Affiliation:(Science Department,Jiangxi Educational Institution,Jiangxi Nanchang 330029,China)
Abstract:Camphor sulfonate was synthesized from camphor sulfoacid by two steps reaction and was charactrized by IR and 1H NMR.The optimum reaction conditions were as follows: n(camphor sulfonyl chloride)∶n(methyl alcohol)∶n(pyridine)=1.0∶2.5∶4.0,reaction temperature-5℃ and reaction time 2 h.The yield of methyl camphor sulfonate was 73.2% with 99.6% purity.
Keywords:methyl camphor sulfonate  ethyl camphor sulfonate  camphor sulfonyl chloride  camphor sulfoacid  chiral auxiliary
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