Imidazolium Zwitterionic Molten Salt: An Efficient Organocatalyst under Neat Conditions at Room Temperature for the Synthesis of Dipyrromethanes as well as Bis(indolyl)methanes

被引:28
作者
Chatterjee, Rana [1 ]
Mahato, Sachinta [1 ]
Santra, Sougata [2 ]
Zyryanov, Grigory V. [2 ,3 ]
Hajra, Alakananda [1 ]
Majee, Adinath [1 ]
机构
[1] Visva Bharati A Cent Univ, Dept Chem, Santini Ketan 731235, W Bengal, India
[2] Ural Fed Univ, Dept Organ & Biomol Chem, Inst Chem Engn, 19 Mira Str, Ekaterinburg 620002, Russia
[3] Russian Acad Sci, I Ya Postovskiy Inst Organ Synth, Ural Div, 22 S Kovalevskoy Str, Ekaterinburg 620219, Russia
基金
俄罗斯科学基金会;
关键词
bis(indolyl)methanes; dipyrromethanes; room temperature; solvent-free; zwitterionic molten salt; NONREARRANGED MONOTERPENOID UNIT; SIMPLE INDOLE ALKALOIDS; SOLVENT-FREE CONDITIONS; CHIRAL IONIC LIQUIDS; CARBONYL-COMPOUNDS; MESOSUBSTITUTED DIPYRROMETHANES; REGIOSELECTIVE SYNTHESIS; CATALYTIC APPLICATION; BIS-INDOLYLMETHANES; MEDIATED SYNTHESIS;
D O I
10.1002/slct.201800227
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An imidazole-based zwitterionic-salt, 4-(3-methylimidazolium)butane sulfonate (MBS), has been found to be an efficient organocatalyst for the synthesis of dipyrromethanes as well as bis(indolyl)methanes at room temperature under solvent-free conditions (neat) in high yields. The reaction procedure is very simple and a large variety of aldehydes have been examined under similar conditions for indoles and pyrroles. The catalytic reaction proceeded very smoothly and showed high chemoselectivity. Clean reaction, ease of product isolation/purification, easily accessible reactants, metal and solvent-free and environmentally friendly reaction conditions are the notable advantages of the present methodology.
引用
收藏
页码:5843 / 5847
页数:5
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