王文琛, 杨志翔, 王金娟, 尹晓刚, 陈治明. MMT/FeCl3催化下微波法合成双吲哚甲烷衍生物[J]. 云南大学学报(自然科学版), 2018, 40(2): 341-346. doi: 10.7540/j.ynu.20170408
引用本文: 王文琛, 杨志翔, 王金娟, 尹晓刚, 陈治明. MMT/FeCl3催化下微波法合成双吲哚甲烷衍生物[J]. 云南大学学报(自然科学版), 2018, 40(2): 341-346. doi: 10.7540/j.ynu.20170408
WANG Wen-cheng, YANG Zhi-xiang, WANG Jin-juan, YIN Xiao-gang, CHENG Zhi-ming. Synthesis of bis(indol-3-yl)methanes catalyzed by MMT/FeCl3 under microwave irradiation[J]. Journal of Yunnan University: Natural Sciences Edition, 2018, 40(2): 341-346. DOI: 10.7540/j.ynu.20170408
Citation: WANG Wen-cheng, YANG Zhi-xiang, WANG Jin-juan, YIN Xiao-gang, CHENG Zhi-ming. Synthesis of bis(indol-3-yl)methanes catalyzed by MMT/FeCl3 under microwave irradiation[J]. Journal of Yunnan University: Natural Sciences Edition, 2018, 40(2): 341-346. DOI: 10.7540/j.ynu.20170408

MMT/FeCl3催化下微波法合成双吲哚甲烷衍生物

Synthesis of bis(indol-3-yl)methanes catalyzed by MMT/FeCl3 under microwave irradiation

  • 摘要: 探究一种微波辅助MMT/FeCl3催化吲哚与芳香醛的反应,方便、快速地合成双吲哚甲烷衍生物.研究表明,在CH2Cl2中,微波辅助x=15% MMT/FeCl3催化,产率最高可达94%.催化剂重复使用4次,产率仍可达60%.该方法具有操作简单、反应快、产率高、环境友好等优点,为合成双吲哚甲烷衍生物提供了一条有效途径.

     

    Abstract: A rapid and efficient microwave-assisted method for the synthesis of bis(indol-3-yl)methane by the reaction of indoles with aromatic aldehyde catalyzed by Montmorillonite FeCl3 has been developed.The reaction was efficiently performed in the presence of MMT/FeCl3 (x=15%) in CH2Cl2 with high yield up to 94%.The catalyst was reused 4 times and the yield was still up to 60 %.This protocol has the advantages of simple operation,short reaction times,high yields and environmental friendliness,the method is the efficient approach for the synthesis of bis(indol-3-yl)methanes.

     

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