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Lewis酸催化三组分合成喹啉-2,4-二羧酸酯类化合物*

程正载 Mario Gauthier 王云 谢聪 唐然 王涵鼎 丁玲 刘锋波 颜晓潮 朱三勇

湖南大学学报(自然科学版)2018,Vol.45Issue(6):133-138,6.
湖南大学学报(自然科学版)2018,Vol.45Issue(6):133-138,6.DOI:10.16339/j.cnki.hdxbzkb.2018.06.020

Lewis酸催化三组分合成喹啉-2,4-二羧酸酯类化合物*

Synthesis of Quinoline-2,4-dicarboxylate Compounds Based on Three-Component Coupling Catalyzed by Lewis Acid

程正载 1Mario Gauthier 2王云 1谢聪 1唐然 3王涵鼎 1丁玲 1刘锋波 1颜晓潮 1朱三勇1

作者信息

  • 1. 武汉科技大学 化学与化工学院 精细有机化工与有机材料研究所,湖北 武汉 430081
  • 2. 弗罗里达大学 化学系,盖恩斯威尔 32611
  • 3. 湖北科技学院 湖北省非动力核技术协同创新中心,湖北 咸宁 437100
  • 折叠

摘要

Abstract

An efficient method for synthesizing quinoline-2,4-dicarboxylate compounds was developed via a one-pot reaction of catalyzed lewis acid such as cheap and easily obtained AlCl3,CuCl2 and FeCl3 in-stead of aromatic amines,ethyl glyoxylate and methyl pyruvate.The major products were separated and purified by thin-layer chromatography,and their structures were characterized by FT-IR,1H NMR,13C NMR and elemental analysis.The reaction mechanism and the influence of substituents attached to aro-matic amine for the reaction were discussed,which will provide a useful reference for molecular design and synthesis of this kind of novel compounds in the future.This method has some advantages such as cheap materials,mild reaction conditions,high atom economy and high yield.[12]GANDEEPAN P,RAJAMALLI P.Synthesis of substituted quinolines by iron(Ⅲ)-catalyzed three-component coupling re-action of aldehydes,amines,and styrenes[J].Asian Journal of Organic Chemistry,2014,3(3):303-308.

关键词

芳胺/乙醛酸乙酯/丙酮酸甲酯/Lewis酸/喹啉衍生物

Key words

aromatic amine substitution/ethyl glyoxylate/methyl pyruvate/Lewis acid/quinoline de-rivatives

分类

化学化工

引用本文复制引用

程正载,Mario Gauthier,王云,谢聪,唐然,王涵鼎,丁玲,刘锋波,颜晓潮,朱三勇..Lewis酸催化三组分合成喹啉-2,4-二羧酸酯类化合物*[J].湖南大学学报(自然科学版),2018,45(6):133-138,6.

基金项目

湖北省自然科学基金资助项目(2017CFB680),National Natural Science Foundation of Hubei Province(2017CFB680) (2017CFB680)

湖北省教育厅中青年人才项目(Q20162806) (Q20162806)

煤转化与新型炭材料湖北省重点实验室开放基金资助项目(WKDM201509) (WKDM201509)

国家大学生科学基金资助项目(201510488004). (201510488004)

湖南大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1674-2974

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