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食用香料邻氨基苯甲酸乙酯的合成
引用本文:夏世威,郑时国,廖崇刚,张治国,詹豪强.食用香料邻氨基苯甲酸乙酯的合成[J].广东化工,2012,39(9):75-76.
作者姓名:夏世威  郑时国  廖崇刚  张治国  詹豪强
作者单位:西华师范大学化学化工学院化学合成与污染控制四川省重点实验室,四川南充,637009
基金项目:西华师范大学科研启动经费项目
摘    要:文章以邻甲基苯胺为原料经酰胺化,氧化,水解,酯化反应合成了一种食用香料邻氨基苯甲酸乙酯,总收率为64.9%,并通过核磁共振氢谱确定了其结构。该方法所采用的原料价格便宜,反应条件比较温和,每一步反应产物易分离,总产率较高。

关 键 词:食用香料  邻氨基苯甲酸乙酯  合成  酯化反应

Synthesis of Food Flavor Ethyl-o-aminobenzoate
Xia Shiwei,Zheng Shiguo,Liao Chonggang,Zhang Zhiguo,Zhan Haoqiang.Synthesis of Food Flavor Ethyl-o-aminobenzoate[J].Guangdong Chemical Industry,2012,39(9):75-76.
Authors:Xia Shiwei  Zheng Shiguo  Liao Chonggang  Zhang Zhiguo  Zhan Haoqiang
Affiliation:(Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637009, China)
Abstract:In the paper, the food flavor ethyl-o-aminobenzoate was synthesized in the total yield of 64.9 % through amidation, oxidation, hydrolysis and esterification reaction using toluidine as a starting material. Its structure was determined by ~HNMR. The synthetic method was developed by cheap materials, milder reaction conditions, convenient product separation of each reaction step, higher total yield.
Keywords:food flavor  ethyl-o-aminobenzoate  synthesis: esterificationreaction
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