白藜芦醇、白皮杉醇和赤松素的合成  

Synthesis of Resveratrol,Piceatannol and Pinosylvin

作　　者：张静静[1,2] 姚明 李立 桑大永 熊航行[1,2] 刘生鹏 Zhang Jingjing;Yao Ming;Li Li;Sang Dayong;Xiong Hangxing;Liu Shengpeng(School of Chemical Engineering and Pharmacy,Wuhan Institute of Technology,Wuhan 430205;College of Chemical Engineering and Pharmacy,Jingchu University of Technology,Jingmen 448000)

机构地区：[1]武汉工程大学化工与制药学院,武汉430205 [2]荆楚理工学院化工与药学院,荆门448000

出　　处：《有机化学》2020年第4期1062-1067,共6页Chinese Journal of Organic Chemistry

基　　金：湖北省高校优秀中青年科技创新团队(No.T201719)资助项目.

摘　　要：研究了白藜芦醇、赤松素和白皮杉醇的一种简便合成方法.二苯乙烯类化合物在铝和碘的作用下实现双键顺反异构和芳甲醚甲基的脱除,实现白藜芦醇、赤松素和白皮杉醇的高效合成,反应的总收率分别为68%,78%和56%.反应溶剂过滤后可以再次使用.通过量子化学计算和控制实验认为碘自由基可能是脱甲基过程中导致双键顺反异构的关键因素.A convenient method for the practical synthesis of resveratrol,piceatannol and pinosylvin is described.Resveratrol,pinosylvin and piceatannol can be achieved through a simultaneous demethylation and isomerization process from stilbenes with the aid of aluminum and iodine.The overall yields of the reaction were 68%,78%and 56%(based on aromatic aldehyde).The solvent of the reaction can be reused after filtered.At the same time,quantum chemical calculations and control experiments show that iodine radical may be the key factor leading to cis-trans isomerization of double bond in the process of demethylation.

关 键 词：白藜芦醇 二苯乙烯 脱甲基 WITTIG反应 顺反异构 

分 类 号：TQ28[化学工程—有机化工]