Ionic Liquid and Sulfonic Acid Based Bifunctional Periodic Mesoporous Organosilica (BPMO-IL-SO3H) as a Highly Efficient and Reusable Nanocatalyst for the Biginelli Reaction

被引:83
|
作者
Elhamifar, Dawood [1 ]
Nasr-Esfahani, Masoud [1 ]
Karimi, Babak [2 ]
Moshkelgosha, Ramin [1 ]
Shabani, Ahmad [1 ]
机构
[1] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran
[2] IASBS, Dept Chem, Zanjan 451376731, Iran
基金
美国国家科学基金会;
关键词
aldehydes; Biginelli reaction; ionic liquids; mesoporous organosilicas; supported sulfonic acid; SOLVENT-FREE CONDITIONS; ONE-POT SYNTHESIS; HETEROGENEOUS CATALYST; RECYCLABLE CATALYST; COUPLING REACTION; IMPROVED PROTOCOL; RECENT PROGRESS; SILICA-GEL; PMO-IL; FRAMEWORK;
D O I
10.1002/cctc.201402162
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic application of a novel ionic liquid and sulfonic acid based bifunctional periodic mesoporous organosilica (BPMO-IL-SO3H) in the one-pot Biginelli reaction was developed. The BPMO-IL-SO3H catalyst was first prepared by hydrolysis and co-condensation of tetramethoxysilane, 1,3-bis(trimethoxysilylpropyl)-imidazolium iodide and 3-mercaptopropyl-trimethoxysilane in the presence of surfactant template under acidic conditions followed by oxidation of SH groups in the presence of hydrogen peroxide. This catalyst was then characterized by thermal gravimetric analysis, transmission electron microscopy, small-angle powder X-ray diffraction, and nitrogen sorption analysis. The performance of the BPMO-IL-SO3H catalyst was investigated in the Biginelli condensation of a variety of different aldehydes with alkylacetoacetates and urea under solvent-free conditions. The catalyst exhibited excellent activity and delivered corresponding Biginelli products in high to excellent yields and selectivities. Moreover, the reactivity, reusability, and stability of the BPMO-IL-SO3H were also investigated under the applied reaction conditions. Our study showed that the catalyst could be recovered and reused at least 10times without any significant decrease in efficiency.
引用
收藏
页码:2593 / 2599
页数:7
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