应用化学

• 研究论文 • 上一篇    下一篇

双吲哚烷基类化合物在无催化剂和无溶剂条件下的高效合成

刘雄伟1,潘博文1,郭丰敏1,曹煜2,刘雄利1,周英1*   

  1. (1.贵州大学生命科学学院,贵州省中药民族药创制工程中心 贵阳 550025;
    2.贵阳医学院附属医院皮肤科 贵阳 550025)
  • 收稿日期:2013-08-28 修回日期:2013-12-04 出版日期:2014-07-10 发布日期:2014-07-10
  • 通讯作者: 周英,教授; Tel:0851-3851091; Fax:0851-8292184; E-mail:yingzhou71@yeah.net; 研究方向:中药民族药的活性成分提取分离及其结构衍生与活性研究
  • 基金资助:
    贵州大学引进人才科研项目[贵大人基合字(2013)013号] 教育部“新世纪人才支持计划”[教技函(2011)95号]贵州民族药物中新颖活性组分的结构测定及NMR谱仪的应用研发项目(2011YQ12003506)贵州省中药现代化科技产业研究开发专项项目[黔科合中药(2012)5018号]资助

Efficient Synthesis of Bis(indolyl)methanes Under Solvent-free and Catalyst-free Conditions

LIU Xiongwei1, PAN Bowen1, GUO Fengmin1, CAO Yu2, LIU Xiongli1, ZHOU Ying1*   

  1. (1.Guizhou Province Chinese Medicine and Ethnic Medicine Creation Engineering Center,
    College of Life Sciences,Guizhou University,Guiyang 550025,China;
    2.Skin Department,Hospital Affiliated to Guiyang Medical College,Guiyang 550025,China)
  • Received:2013-08-28 Revised:2013-12-04 Published:2014-07-10 Online:2014-07-10

摘要: 在不加催化剂和溶剂条件下,由取代吲哚和取代苯甲醛合成15个已知的双吲哚烷基化合物,反应无溶剂污染,反应条件温和,收率为65%~91%。 讨论了反应速度和取代基的关系,探讨了缩合反应的机理。 并用1H NMR、13C NMR、IR和HRMS等技术手段确定了产物结构。

关键词: 醛, 双吲哚烷基类化合物, 吲哚

Abstract: Without the addition of catalysts and solvents, 15 known bis(indolyl)alkane compounds were synthesized under mild conditions from substituted indoles and substituted benzaldehydes in 65%~91% yields. The mechanism of this condensation reaction was discussed and the relationship between reaction speed and substituent groups was described. All the compounds synthesized were confirmed by 1H NMR, 13C NMR and IR analysis.

Key words: Aldehyde, bisindolylalkane, indole

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