Multicomponent Reaction

Post date: Dec 3, 2018 7:28:56 AM

An interesting multicomponent reaction using first year organic chemistry principles.

https://pubs.acs.org/doi/10.1021/sc300173z

Amberlyst A21 Catalyzed Chromatography-Free Method for Multicomponent Synthesis of Dihydropyrano[2,3-c]pyrazoles in Ethanol

Manisha Bihani, Pranjal P. Bora, Ghanashyam Bez*, and Hassan Askari

Department of Chemistry, North Eastern Hill University, Shillong 793022, India

ACS Sustainable Chem. Eng., 2013, 1 (4), pp 440–447

DOI: 10.1021/sc300173z

Publication Date (Web): February 24, 2013

Copyright © 2013 American Chemical Society

*Fax: +91-364-2558014. Tel: +91-364-2722624. E-mail: ghanashyambez@yahoo.com; bez@nehu.ac.in.

Amberlyst A21 was found to be an extremely efficient catalyst for synthesis of a series of 6-amino-4-alkyl/aryl-3-methyl-2,4-dihydropyrano[2,3-c]pyrazole-carbonitriles by a four-component reaction of a mixture of ethyl acetoacetate, hydrazine hydrate, aldehyde, and malononitrile in ethanol at room temperature. The catalytic efficiency of Amberlyst A21 was compared with some other resin-bound free and anionic bases in order to ascertain the best catalyst for the said conversion. The catalyst was found to work extremely well also for acyclic/cyclic ketones to give corresponding dihydropyrano[2,3-c]pyrazoles or their spirocyclic variants. Easy recovery of the catalyst and its reusability, room temperature reaction conditions, short reaction time, excellent yields, no chromatographic purification, and evasion of environmentally hazardous solvents in the entire reaction process may make this protocol very useful for academia and industry.