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由1,1-二溴烯烃一锅法合成1,4-二取代-1,2,3-三氮唑
引用本文:苏长会,刘霞,潘涛,沈宏,黄兆琴. 由1,1-二溴烯烃一锅法合成1,4-二取代-1,2,3-三氮唑[J]. 化学通报, 2019, 82(12): 1130-1133
作者姓名:苏长会  刘霞  潘涛  沈宏  黄兆琴
作者单位:南京大学金陵学院化学与生命科学学院 南京210089;江苏开放大学环境生态学院 南京210036
基金项目:江苏省高校自然科学基金(16KJB150007)
摘    要:以1,1-二溴乙烯和芳基叠氮化合物为原料,碘化亚铜为催化剂,室温下通过一锅法合成了1,4-二取代-1,2,3-三氮唑衍生物。考察了催化剂用量、反应溶剂、反应温度对产品收率的影响。通过IR,MS,1H NMR及13C NMR等对目标产物结构进行确证,并提出了可能的反应机理。该合成方法具有环境友好、条件温和、操作简单、收率高等特点。

关 键 词:1  1-二溴烯烃  一锅法合成  2  3-三氮唑  杂环化合物
收稿时间:2019-07-16
修稿时间:2019-09-24

One-Pot Synthesis of 1,4-Disubstituted 1,2,3-Triazoles from 1,1-Dibromoalkenes
SU Chang-hui,LIU Xi,PAN Tao,SHEN Hong and HANG Zao-qin. One-Pot Synthesis of 1,4-Disubstituted 1,2,3-Triazoles from 1,1-Dibromoalkenes[J]. Chemistry, 2019, 82(12): 1130-1133
Authors:SU Chang-hui  LIU Xi  PAN Tao  SHEN Hong  HANG Zao-qin
Affiliation:School of Chemistry and Life Science,Nanjing University Jinling College,Nanjing,Jiangsu,College of Environment Science and ecology,Jiangsu Open University,Nanjing,Jiangsu,College of Environment Science and ecology,Jiangsu Open University,Nanjing,Jiangsu,College of Environment Science and ecology,Jiangsu Open University,Nanjing,Jiangsu,College of Environment Science and ecology,Jiangsu Open University,Nanjing,Jiangsu
Abstract:1,4-Disubstituted 1,2,3-Triazoles were synthesized by a CuI catalysed one-pot reaction using 1,1-dibromoalkenes and aryl azides as raw materials under room temperature. Effects of the amount of catalyst, solvent and the reaction temperature on the yields of product were studied. The structures of the 1,2,3-Triazoles were characterized by IR analysis, mass spectrometry, 1H NMR and 13C NMR spectroscopy. A mechanism to rationalize the reaction was proposed. This method has the advantages of environment friendly, mild reaction conditions, simple one pot operation and high yields.
Keywords:1,1-Dibromoalkene   One-pot synthesis   1,2,3-Triazoles   Heterocycles
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