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An efficient strategy to synthesis of β-carbonyl compounds by 1-pentyl-1,2,4-triazolium methanesulfonate

Publication Type : Conference Proceedings

Publisher : Materials Today: Proceedings

Source : Materials Today: Proceedings, Volume 33, p.2144-2147 (2020)

Url : https://www.sciencedirect.com/science/article/pii/S2214785320319064

Keywords : 1, 2, 4-triazole, Green chemistry, Ionic liquids, Triazolium salts, β-amino carbonyl compounds

Campus : Coimbatore

School : School of Engineering

Department : Sciences

Year : 2020

Abstract : It is well known that applying green chemistry aspects for organic reactions would reduce the toxicity of chemicals and it reduces the amount of volatile organic solvents too. Thus we have developed a Bronsted acidic 1-pentyl-1,2–4-triazolium methanesulfonate as a room temperature ionic liquid for organic reactions as reaction medium. The same has been employed as organocatalyst for the synthesis of β-Carbonyl Compounds. The present papers reveal the significance of ionic liquids in optimization of reaction condition in terms of equivalence of reagents, impact of solvents and amount of catalyst, synthesis of library of halogen rich β-carbonyl compounds.

Cite this Research Publication : S. Paramparambath, Selvam, S., Puthukkudy, G., Satheesh, A., and Dr. Elango K., “An efficient strategy to synthesis of β-carbonyl compounds by 1-pentyl-1,2,4-triazolium methanesulfonate”, Materials Today: Proceedings, vol. 33. pp. 2144-2147, 2020.

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