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Knoevenagel Reaction Catalyzed by a Reusable Bronsted Acid Based on 1-Alkyl-1,2,4-triazolium Tetrafluoroborate

Publication Type : Journal Article

Publisher : Letters in Organic Chemistry

Source : Letters in Organic Chemistry, Volume 15, Issue 2 (2018)

Url : http://www.eurekaselect.com/node/156453/article

Keywords : Aldehyde, benzylidenemalononitrile, Brønsted acid, Ionic liquids, Knoevenagel reaction, reusable catalyst, salts., triazolium

Campus : Coimbatore

School : School of Engineering

Department : Sciences

Year : 2018

Abstract : The Knoevenagel reaction is one of the most useful methods for the synthesis of α,β-unsaturated nitriles. We disclose an efficient protocol for the Knoevenagel reaction of aldehydes withmalononitrile catalyzed by 1-alkyl-1,2,4-triazolium salts to afford the corresponding products in excellentyields. The important feature of this reaction is the catalyst; 1-alkyl-1,2,4-triazolium salts are recycledand reused. Furthermore, the reaction conditions are environment friendly and do not produce anyhazardous waste.

Cite this Research Publication : Dr. Elango K., Nagarajan, S., and Shaikh, T. M., “Knoevenagel Reaction Catalyzed by a Reusable Bronsted Acid Based on 1-Alkyl-1,2,4-triazolium Tetrafluoroborate”, Letters in Organic Chemistry, vol. 15, no. 2, 2018.

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