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点击化反应合成8-(4-苯基-1,2,3-三氮唑)-喹啉
引用本文:张慧梓,范逸平. 点击化反应合成8-(4-苯基-1,2,3-三氮唑)-喹啉[J]. 化工时刊, 2011, 25(2): 39-41. DOI: 10.3969/j.issn.1002-154X.2011.02.011
作者姓名:张慧梓  范逸平
作者单位:云南民族大学,民族药资源国家重点实验室,云南,昆明,650500
摘    要:以喹啉为原料,经改进Skraup法合成了8-羟基喹啉,再合成8-氯喹啉,最终利用点击反应,合成总产物.采用相转移催化剂,水作为溶剂和价廉的Cu(I)为催化剂,常温下-锅制得产物,并且产率高达90%.

关 键 词:8-(4-苯基-1,2,3-三氮唑)-喹啉  点击化学  合成

Synthesis of 8-(4-phenyl-1H-1,2,3-triazol-1-y1) Quinoline with Click Chemistry
Zhang Huizi,Fan Yiping. Synthesis of 8-(4-phenyl-1H-1,2,3-triazol-1-y1) Quinoline with Click Chemistry[J]. Chemical Industry Times, 2011, 25(2): 39-41. DOI: 10.3969/j.issn.1002-154X.2011.02.011
Authors:Zhang Huizi  Fan Yiping
Affiliation:Zhang Huizi Fan Yiping(YunNan Nationnalities University,Key Laboratory of National Medicine Resources, Yunnan Kunming 650500)
Abstract:Quinoline as raw materials,Synthesis of 8-hydroxyquinoline by improved Skraup method,and then synthesis of 8-chloroquinoline,the ultimate get the product 8-(4-phenyl-1H-1,2,3-triazol-1-yl)quinoline by click reaction,In this study,the low cost catalysts,phase transfer catalyst,water and Cu(I) were used,get the product with "one pot reaction" at room temperature,and yield up to 90%.
Keywords:8-(4-phenyl-1H-1  2  3-triazol-1-yl)quinoline click chemistry synthesis
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