Solvent-free synthesis of quinoline derivatives via the Friedlander reaction using 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and recyclable ionic liquid catalyst

被引：33

作者：

Shirini, Farhad ^{[1
]}

Yahyazadeh, Asieh ^{[1
]}

Mohammadi, Kamal ^{[1
]}

Khaligh, Nader Ghaffari ^{[1
]}

机构：

[1] Univ Guilan, Coll Sci, Dept Chem, Rasht 41335, Iran

来源：

COMPTES RENDUS CHIMIE | 2014年 / 17卷 / 04期

关键词：

Quinolines; Ionic liquid; Friedlander annulation; Solvent-free conditions; ONE-STEP SYNTHESIS; CONJUGATED POLYMERS; MEDIATED SYNTHESIS; HIGHLY EFFICIENT; IN-VITRO; MILD; ELECTROLUMINESCENCE; ESTERIFICATION; INHIBITORS; ANNULATION;

D O I：

10.1016/j.crci.2013.10.007

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A convenient, highly versatile and eco-friendly protocol for the synthesis of quinoline derivatives via the Friedlander reaction is presented. The method is based on the use of 1,3-disulfonic acid imidazolium hydrogen sulfate (DSIMHS) as an efficient and reusable ionic liquid catalyst. A variety of ketones afforded the substituted quinolines in excellent yields during relatively short reaction times under solvent-free conditions; ithe catalyst could be easily recovered and reused for several times without any appreciable loss of activity. (C) 2013 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.

引用

页码：370 / 376

页数：7

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