Journal
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY
Volume 13, Issue 2, Pages 267-277Publisher
SPRINGER
DOI: 10.1007/s13738-015-0734-5
Keywords
Biginelli reaction; Hantzsch reaction; Green synthesis; Metal-supported nanocatalysts; Polysubstituted pyridines; Oxidative aromatization
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Funding
- University of Tabriz
- Iranian Nanotechnology Initiative
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In this work, catalyst composition-activity relationship of supported catalysts in Biginelli and Hantzsch reactions was investigated under mild conditions. Biginelli dihydropyrimidinone/thiones were prepared over Fe-Cu/ZSM-5 as an efficient, convenient, and environmentally benign catalyst under ultrasonic irradiation in aqueous media in very good yields. The Fe-Cu/ZSM-5-catalyzed synthesis of 1,4-dihydropyridines and their aromatization to polysubstituted pyridines and also a new one-pot, two-step, and sequential protocol for the synthesis of pyridine derivatives, employing an aldehyde, ethyl acetoacetate, and ammonium acetate under the same green experimental conditions were illustrated. Three-component condensation in the presence of supported reagent with operational simplicity, inexpensive reagents, short reaction time, high yield of products, and use of non-toxic reagents makes this synthetic protocol an attractive one.
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