Type: Article
Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives
Journal: Organic Letters (15237052)Year: 2 October 2015Volume: 17Issue: Pages: 4666 - 4669
DOI:10.1021/acs.orglett.5b01837Language: English
Abstract
A regioselective green synthesis of nitroacetaminophen derivatives was carried out by electrochemical oxidation of acetaminophen, N-(2-hydroxyphenyl)acetamide, and 1-(4-(4-hydroxyphenyl)piperazin-1-yl)ethanone in the presence of nitrite ion as a nucleophile. The present work has led to the development of a reagentless green and facile electrochemical method for the synthesis of some nitroacetaminophen derivatives. © 2015 American Chemical Society.
Other Keywords
AcetaminophenAcetanilidesMolecular StructureNitratesPiperazinesStereoisomerism1-(4-(4-hydroxyphenyl)piperazin-1-yl)ethanone2-hydroxyacetanilide4-(nitroxy)butanoic acid 4-acetylaminophenyl esteracetanilide derivativenitric acid derivativeparacetamolpiperazine derivativeanalogs and derivativeschemical structurechemistrysynthesis