Synthesis of 2,4,5-trisubstituted imidazoles, quinoxalines and 1,5-benzodiazepines over an eco-friendly and highly efficient ZrO2-Al2O3 catalyst

被引:39
|
作者
Thimmaraju, N. [1 ,2 ]
Shamshuddin, S. Z. Mohamed [1 ,2 ]
机构
[1] HMS Inst Technol, Chem Res Lab, Tumkur 572104, Karnataka, India
[2] Bharathiar Univ, Res & Dev Ctr, Coimbatore, Tamil Nadu, India
来源
RSC ADVANCES | 2016年 / 6卷 / 65期
关键词
ONE-POT SYNTHESIS; TETRASUBSTITUTED IMIDAZOLES; GREEN SYNTHESIS; 1,2,4,5-TETRASUBSTITUTED IMIDAZOLES; MULTICOMPONENT REACTIONS; REUSABLE CATALYST; RAPID SYNTHESIS; ZIRCONIA; ACID; TRANSESTERIFICATION;
D O I
10.1039/c6ra13956f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
ZrO2-Al2O3 containing 80 mol% of ZrO2 was prepared by solution combustion, impregnation and precipitation methods. All the prepared catalytic materials were characterized by PXRD, NH3-TPD, N-2 adsorption isotherms, FTIR, TEM, SEM, EDAX and ICP-OES techniques. These catalytic materials were used in a rapid, simple, versatile and efficient synthesis of 2,4,5-trisubstituted imidazoles under solvent-free conditions at moderate temperature in shorter reaction time (20 min). This is achieved by three-component cyclo-condensation of benzil, aldehydes and ammonium acetate in excellent yields. The derivatives of quinoxalines and 1,5-benzodiazepines were synthesized effectively by cyclo-condensation of 1,2-diamine with alpha-diketones and carbonyl compound with O-phenylenediamines respectively over ZrO2-Al2O3 at moderate temperature (80 degrees C) for the reaction time of 20-40 min in presence of ethanol as a solvent. The present method is experimentally simple, non-toxic and involves inexpensive reagents, clean reaction pathways and an eco-friendly catalyst. The catalytic materials used can be easily separated from the reaction mixture and reused for several reaction cycles without much loss of catalytic activity.
引用
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页码:60231 / 60243
页数:13
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