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钌/酸共催化邻氨基苯甲醇和芳基端炔合成喹啉衍生物
引用本文:刘建本,陈上. 钌/酸共催化邻氨基苯甲醇和芳基端炔合成喹啉衍生物[J]. 应用化学, 2015, 32(3): 267-272. DOI: 10.11944/j.issn.1000-0518.2015.03.140250
作者姓名:刘建本  陈上
作者单位:吉首大学化学化工学院 湖南 吉首 416000
摘    要:以邻氨基苯甲醇为原料进行催化脱氢反应,经过对催化体系的一系列筛选,最终采用[RuCl2(p-cymene)]2/AgOTf共催化体系,使邻氨基苯甲醇发生催化脱氢和芳基端炔发生交叉偶联反应,并以39%~47%的收率获得合成一系列2-芳基喹啉衍类生物,发展了邻氨基苯甲醇与芳基末端炔烃合成喹啉衍类生物的新方法,是对喹啉类衍生物合成方法的一个重要补充。

关 键 词:钌催化  邻氨基苯甲醇  脱氢  喹啉类衍生物  
收稿时间:2014-07-18

Ruthenium/Acid Co-catalyzed Synthesis of Quinoline Derivatives from o-Aminoarylmethanols and Terminal Arylalkynes
LIU Jianben,CHEN Shang. Ruthenium/Acid Co-catalyzed Synthesis of Quinoline Derivatives from o-Aminoarylmethanols and Terminal Arylalkynes[J]. Chinese Journal of Applied Chemistry, 2015, 32(3): 267-272. DOI: 10.11944/j.issn.1000-0518.2015.03.140250
Authors:LIU Jianben  CHEN Shang
Affiliation:College of Chemistry and Chemical Engineering,Jishou University,Jishou,Hu'nan 416000,China
Abstract:By using o-aminophenyl methanol as the starting material and undergoing a dehydrogenation reaction, [RuCl2(p-cymene)]2/AgOTf was finally employed as the co-catalyst system upon a systematical screening of catalysts, which enables the dehydrogenation of o-aminophenyl methanol to undergo a cross-coupling reaction with terminal aryl alkynes, affording a series of 2-aryl quinolines in 39% to 47% yields. The study has demonstrated a new method for the synthesis of quinolines from o-aminophenyl methanol and terminal aryl alkynes, which is an important complement to the synthesis of quinoline derivatives.
Keywords:ruthenium catalysis  o-aminoaryl methanol  dehydrogenation  quinoline derivatives
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