Acetophenone Mannich bases: study of ionic liquid catalysed synthesis and antioxidative potential of products.

ABSTRACT: Three-component Mannich reaction of acetophenone or 4-iodoacetophenone with a variety of substituted anilines and benzaldehyde, catalysed with diethanolammonium chloroacetate, was performed under mild conditions. Mannich bases (MBs), of which five are new, were obtained in good to excellent yields. All compounds were characterized using elemental analysis, NMR and IR. In addition, detailed experimental and simulated UV-Vis spectral characterization of these compounds is presented here for the first time. In vitro antioxidative potential of synthetized MBs was evaluated using 2,2-diphenyl-1-picryl-hydrazyl radical and density functional theory (DFT) thermodynamical study. It was shown that compounds with anisidine moiety express moderate antioxidative activity. Mechanism of the organocataly

SUBMITTER: Petrovic VP 

PROVIDER: S-EPMC6281942 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature