Bifunctional C2-symmetric ionic liquid-supported (S)-proline as a recyclable organocatalyst for Mannich reactions in neat condition

A bi-functional C2-symmetric ionic liquid-supported (S)-Proline organocatalyst [BHEDIMP][CF3CO2] has been designed and synthesized for the first time. The novel C2-symmetric organocatalyst [BHEDIMP][CF3CO2] (4 mol%) was employed for the one-pot multi-component Mannich reactions comprising of substit...

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Bibliographic Details
Main Authors: Prabhakara Madivalappa Davanagere, Barnali Maiti
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Results in Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211715621000576
Description
Summary:A bi-functional C2-symmetric ionic liquid-supported (S)-Proline organocatalyst [BHEDIMP][CF3CO2] has been designed and synthesized for the first time. The novel C2-symmetric organocatalyst [BHEDIMP][CF3CO2] (4 mol%) was employed for the one-pot multi-component Mannich reactions comprising of substituted acetophenones, arylamines, and aryl aldehydes to yield racemic β-amino ketones derivatives in neat conditions. This present synthetic method is highlighted by numerous advantages such as low catalyst loading percentage, solvent-free synthesis, short reaction times, easily accessible substrates, and devoid of chromatography purification. The supported C2-symmetric organocatalyst was recycled and reused six times without substantial damage to its catalytic efficiency.
ISSN:2211-7156