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Simple and solvent free practical procedure for chalcones: An expeditious, mild and greener approach

Duha Adnan, Bijender Singh, S.K. Mehta, Vinod Kumar, Ramesh Kataria

2020Current Research in Green and Sustainable Chemistry31 citationsDOIOpen Access PDF

Abstract

An extremely simple, expeditious and greener synthetic method for a variety of chalcone derivatives (3) under mild and solvent free reaction conditions has been developed. The present protocol discloses the use of p-toluenesulfonic acid (p-TSA) as a solid phase organocatalyst which accelerates the Claisen–Schmidt condensation reaction dramatically under mild conditions. Various aryl aldehydes (1) were treated with differently substituted aryl ketones (2) in the presence of p-TSA at 50–60 ​°C to yield the desired products in a very short period of reaction time. Mild reaction conditions, clean reaction media, expulsion of hazardous solvents, simple work-up, exclusive formation of products in high yields without side products, and easy purification are advantages of the present methodology.

Topics & Concepts

ChalconeChemistryYield (engineering)ArylOrganic chemistryReaction conditionsSolventCondensationCondensation reactionCombinatorial chemistryCatalysisMaterials scienceAlkylThermodynamicsMetallurgyPhysicsSynthesis and biological activitySynthesis and Biological EvaluationMulticomponent Synthesis of Heterocycles
Simple and solvent free practical procedure for chalcones: An expeditious, mild and greener approach | Litcius