期刊
CHEMISTRYSELECT
卷 8, 期 35, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202300754
关键词
Dihydroquinazolinones; Heterogeneous cooperative catalysis; Mesoporous Fe-MCM-41; Supported ionic liquids; Sustainable synthesis
This study presents a successful strategy for the generation of multifunctional heterogeneous supported ionic liquid catalysts and their application in the synthesis of dihydroquinazolinones. The influence of different catalysts and reaction parameters on the catalytic behaviors were investigated, and (2)Fe-MCM-41/IL(0.6) was found to exhibit the optimal catalytic efficiency.
In this study, we report a successful strategy for the generation of a type of multifunctional heterogeneous supported ionic liquids catalysts. The synthesized supported ionic liquids (Fe-MCM-41/IL) were used in the catalytic cyclocondensation of 2-aminobenzamide and various ketones and aldehydes towards the efficient synthesis of the dihydroquinazolinones under green conditions. The influence of the different catalysts and reaction parameters on the catalytic behaviors were sufficiently investigated. The supported catalyst (2)Fe-MCM-41/IL(0.6) showed the optimal catalytic efficiency. A hot filtration experiment revealed that the reaction proceeded in a heterogeneous pathway. The catalytic activity of (2)Fe-MCM-41/IL(0.6) could be maintained efficiently after recycling up to five consecutive runs under the optimized reaction conditions. Merits of this meticulously designed protocol are the use of novel supported catalyst, easy work-up process, feasibility and sustainability, indicating its potential industrial application prospect. A new and simple method for the synthesis of dihydroquinazolinones using Fe-MCM-41-supported titanium tetrachloride-based ionic liquids as heterogeneous catalysts has been reported. The supported cooperative catalyst (2)Fe-MCM-41/IL(0.6) exhibited excellent catalytic activity in the cyclocondensation reaction with good recyclability and reusability up to five consecutive runs without considerable decrease in catalytic activity.image
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