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天然产物5,7-二甲氧基-4′-羟基异黄酮的合成
引用本文:任宛莉,陈东玲,金叶,李洪启.天然产物5,7-二甲氧基-4′-羟基异黄酮的合成[J].化学研究,2009,20(4):10-13.
作者姓名:任宛莉  陈东玲  金叶  李洪启
作者单位:1. 宝鸡职业技术学院医学部,陕西,宝鸡,721006
2. 东华大学化学化工与生物工程学院,生态纺织教育部重点实验室,上海,201620
基金项目:教育部留学回国人员科研启动基金,上海市自然科学基金项目 
摘    要:以4-羟基苯乙酸和3,5-二甲氧基苯酚为原料,通过一条包括苄基化、酰氯化、酯化、氢化、Fries重排、以及Vilsmeier-Haack反应等6步反应的路线合成了天然产物5,7-二甲氧基-4′-羟基异黄酮,目标产物的总收率为33%.利用1HNMR、13C NMR及元素分析确证了化合物的结构.

关 键 词:5  7-二甲氧基-4′-羟基异黄酮  4-羟基苯乙酸  3  5-二甲氧基苯酚  Fries重排  Vilsmeier-Haack反应

Synthesis of Natural Product 5,7-Dimethoxyl-4'-Hydroxyisoflavone
REN Wan-li,CHEN Dong-ling,JIN Ye,LI Hong-qi.Synthesis of Natural Product 5,7-Dimethoxyl-4'-Hydroxyisoflavone[J].Chemical Research,2009,20(4):10-13.
Authors:REN Wan-li  CHEN Dong-ling  JIN Ye  LI Hong-qi
Institution:REN Wan-li, CHEN Dong-ling, JIN Ye, LI Hong-qi ( 1. Medical School, Baoji Vocational and Technological College, Baoji 721006, Shaanxi, China; 2, Key Laboratory of Science & Technology of Eco-Textile, Ministry of Education, College of Chemistry Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, China)
Abstract:The natural product 5,7-dimethoxyl-4′-hydroxyisoflavone was synthesized by using a 6-step synthetic protocol including benzylization,acyl chloride forming reaction,esterification,hydrogenation,Fries transformation and Vilsmeier-Haack reaction with 4-hydroxyphenylacetic acid and 3,5-dimethoxyphenol as the starting materials.The overall yield of the target compound was 33%.The structures of the target compounds were confirmed by 1H NMR,13C NMR and elemental analysis.
Keywords:5  7-dimethoxyl-4′-hydroxyisoflavone  4-hydroxyphenylacetic acid  3  5-dimethoxyphenol  Fries transformation  Vilsmeier-Haack reaction
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