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手性助剂樟脑磺酸酯的合成工艺研究

Studies on Synthesis of Camphor Sulfonate as Chiral Auxiliary
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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%。 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.
出处 《化学世界》 CAS CSCD 北大核心 2012年第5期300-302,共3页 Chemical World
基金 江西省教育厅科技计划项目(赣教科技便函字2002-01)
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 methyl camphor sulfonate ethyl camphor sulfonate camphor sulfonyl chloride camphor sulfoacid chiral auxiliary
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