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L-扁桃酸正丁酯的合成
引用本文:左彬,彭阳峰,赵红亮,童天中.L-扁桃酸正丁酯的合成[J].化学世界,2010,51(11).
作者姓名:左彬  彭阳峰  赵红亮  童天中
作者单位:华东理工大学化工学院,上海,200237
摘    要:以L-扁桃酸与正丁醇为原料,在对甲苯磺酸催化下合成了手性拆分剂L-扁桃酸正丁酯,通过正交实验确定优化反应条件为:L-扁桃酸0.1 mol,n(L-扁桃酸):n(正丁醇)=1∶2,对甲苯磺酸0.1 g,甲苯50 mL,回流反应约5 h,酯化率99%,收率在96%以上。其结构经1H NMR确证。

关 键 词:手性  拆分  扁桃酸  正丁醇  酯化

Synthesis of n-Butyl L-Mandelate
ZUO Bin,PENG Yang-feng,ZHAO Hong-liang,TONG Tian-zhong.Synthesis of n-Butyl L-Mandelate[J].Chemical World,2010,51(11).
Authors:ZUO Bin  PENG Yang-feng  ZHAO Hong-liang  TONG Tian-zhong
Abstract:A chiral resolving reagent,n-butyl L-mandelate,was synthsized from L-mandelic acid and n-buta-nol by refluxing for 5 h using p-toluene sulfonic acid as catalyst.The effect of molar ratio of reactant,amount of solvent and catalyst on the yield were investigated by orthogonal test.The optimum reaction conditions were as follow: L-mandelic acid was 0.1 mol;the molar ratio of L-mandelic acid to n-buta-nol was 1∶2;the amount of p-toluene sulfonic acid was 0.1 g;and toluene was 50 mL.The yield was over 96% and the esterification rate was about 99% under the optimum reaction conditions.The structure of the product was confirmed by()~1H NMR.
Keywords:chiral  resolving  mandelic acid  n-butanol  esterification
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