Friedländer Synthesis of Substituted Quinolines Using an Efficient and Reusable Brønsted Acid Ionic Liquid Supported on Fe۳O۴@SiO۲ Nanoparticles under Solvent-free Conditions
Publish place: Organic Chemistry Research، Vol: 6، Issue: 1
Publish Year: 1399
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_ORGC-6-1_012
تاریخ نمایه سازی: 3 مهر 1402
Abstract:
In this study, a highly efficient and recyclable Brønsted acid ionic liquid, ۱-methyl-۳-(۳-triethoxysilylpropyl)-۱H-imidazol-۳-ium hydrogensulfate, immobilized on the surface of Fe۳O۴@SiO۲ (MNP-IL-HSO۴) was prepared and characterized. Then, the catalytic activity of this nanomagnetic catalyst was investigated in the Friedländer synthesis of substituted quinolines through the cyclocondensation reaction of o-aminoaryl ketones with α-methylene carbonyl compounds under solvent-free conditions. The present protocol has several advantages, including short reaction times, high yield of products, simplicity in operation, simple work-up and reusability of the catalyst.
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Authors
Mehdi Fallah-Mehrjardi
Department of Chemistry, Payame Noor University, Tehran, ۱۹۳۹۵-۴۶۹۷, Iran
Samaneh Kalantari
Department of Chemistry, Payame Noor University (PNU), P.O. Box ۱۹۳۹۵-۳۶۹۷, Tehran, Iran