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

Publication Type : Journal Article

Publisher : Elsevier

Source : Materials Today: Proceedings Volume 33 Pages 2144-2147, 2020

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

Campus : Coimbatore

School : School of Physical Sciences

Department : Department of 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 : Sreedevi Paramparambath, Susithra Selvam, Geethu Puthukkudy, Anjitha Satheesh, Elango Kandasamy, "An efficient strategy to synthesis of β-carbonyl compounds by 1-pentyl-1, 2, 4-triazolium methanesulfonate", Materials Today: Proceedings Volume 33 Pages 2144-2147, 2020

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