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3,5-二乙基-2,4-二甲氧羰基吡咯的合成
引用本文:黄诗,张丽俊,王晓红.3,5-二乙基-2,4-二甲氧羰基吡咯的合成[J].广州化工,2009,37(6):97-98.
作者姓名:黄诗  张丽俊  王晓红
作者单位:江苏大学化工学院,江苏,镇江,212013
摘    要:在制备八乙基咔咯的过程中,得到了一种新的化合物3,5-二乙基-2,4-二甲氧羰基吡咯。它是以丙酰乙酸甲酯为原料,经过亚硝化、还原、与原料自身通过Knorr反应制得产物。研究了不同的反应条件对产率的影响,并提出了最佳反应条件。通过熔点测定、IR和^1HNMR光谱对产物进行了表征。

关 键 词:咔咯中间体  Knott反应  合成

Synthesis of the 3,5-diethyl-2,4-dimethoxycarbonylpyrrole
HUANG Shi,ZHANG Li-jun,WANG Xiao-hong.Synthesis of the 3,5-diethyl-2,4-dimethoxycarbonylpyrrole[J].GuangZhou Chemical Industry and Technology,2009,37(6):97-98.
Authors:HUANG Shi  ZHANG Li-jun  WANG Xiao-hong
Affiliation:HUANG Shi, ZHANG Li -jun, WANG Xiao -hong ( School of Chemistry And Chemical Engineering Jiangsu University, Jiangsu Zhenjiang 212013, China)
Abstract:3,5 - diethyl - 2,4 - dimethoxycarbonylpyrrole, found in the process of synthesis of the octaethylcorrole, was synthesized from methyl 3 - oxo - pentanoate which undegoed a nitrosation and Knorr reaction. Factors affecting the synthesis process of the intermediate were investigated. The product was characterized by melting point measurement, IR and ^1HNMR spectroscopy.
Keywords:the intermediates of corrole  Knorr reaction  synthesis
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