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离子液体中醛与2-(2-苯并咪唑)乙腈的Knoevenagel缩合反应
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  • 英文篇名:Knoevenagel condensation of aldehyde and 2-(1H-benzo[d]imidazol-2-yl) acetonitrile in ionic liquids
  • 作者:吕兰兰 ; 张梅梅 ; 刘建全
  • 英文作者:Lü Lanlan;Zhang Meimei;Liu Jianquan;School of Chemistry & Materials Science,Jiangsu Normal University;
  • 关键词:2-(2-苯并咪唑)乙腈 ; Knoevenagel反应 ; 离子液体 ; 合成
  • 英文关键词:2-(1H-benzo[d]imidazol-2-yl) acetonitrile;;Knoevenagel condensation;;ionic liquids;;synthesis
  • 中文刊名:XZSX
  • 英文刊名:Journal of Jiangsu Normal University(Natural Science Edition)
  • 机构:江苏师范大学化学与材料科学学院;
  • 出版日期:2019-02-15
  • 出版单位:江苏师范大学学报(自然科学版)
  • 年:2019
  • 期:v.37;No.127
  • 基金:江苏师范大学优秀博士人才引进项目(16XLR013)
  • 语种:中文;
  • 页:XZSX201901017
  • 页数:4
  • CN:01
  • ISSN:32-1834/N
  • 分类号:74-77
摘要
以离子液体作为绿色反应介质,醛和2-(2-苯并咪唑)乙腈为原料,80℃发生Knoevenagel缩合反应,选择性合成了一系列的(E)-2-(2-苯并咪唑)-3-芳基丙烯腈衍生物.和其他方法相比,该方法具有反应条件温和、产率高(86%~95%)和环境友好等优点.产物的结构均通过熔点、红外、氢谱和高分辨质谱加以确证.
        A series of (E)-2-(1 H-benzo[d]imidazol-2-yl)-3-arylacrylonitrile derivatives are synthesized by a Knoevenagel condensation of 2-(1 H-benzo[d]imidazol-2-yl)acetonitrile and aromatic aldehyde at 80 ℃ in ionic liquids.Compared to the other methods,this method has the advantages of milder reaction conditions,high yields(86%~95%)and environmental benignity.The structures of the products are characterized by melting points,IR,1 HNMR and HRMS.
引文
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