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5,10,15,20-中位-四(4-氨基苯基)卟吩合成方法的改进
引用本文:李和平,郭灿城.5,10,15,20-中位-四(4-氨基苯基)卟吩合成方法的改进[J].有机化学,2000,20(5):830-832.
作者姓名:李和平  郭灿城
作者单位:湖南大学化学化工学院,长沙,410082
摘    要:在还原剂维生素C存在下,将4-氨基苯甲醛与吡咯在丙酸中缩合得到5,10,15,20-中位-四(4-氨基苯基)卟吩,操作简单,产率高于文献方法。

关 键 词:缩合反应  卟吩P  苯甲醛P  维生素C
修稿时间:2000年1月6日

An improved synthetic method for preparing 5,10,15,20-meso-tetra(4- aminophenyl)porphine
LI He-Ping,GUO Can-Cheng.An improved synthetic method for preparing 5,10,15,20-meso-tetra(4- aminophenyl)porphine[J].Chinese Journal of Organic Chemistry,2000,20(5):830-832.
Authors:LI He-Ping  GUO Can-Cheng
Abstract:An improved Adler method for preparing 5, 10, 15, 20 - meso - tetra(4 - aminophenyl) porphine ( TAPPH2 ) is presented. TAPPH2 was synthesized by direct condensation of pyrrole with 4 - aminobenzaldehyde in reflux-ing propanoic acid in the presence of vitamin C. This new synthetic strategy for preparing TAPPH2 should greatly expand synthetic entries to porphines containing atnino groups. As a complementary to the Adler procedure this methodology allows forpreparation of aminophenylporphines from sensitive aminobenzaldehydes in ca 20% yields without suffering from difficult purification problems.
Keywords:4 - aminobenzaldehyde  5  10  15  20 - meso - tetra (4 - aminophenyl)porphine  synthesis  
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