Carboxylation of hydroxyarens with metal alkyl carbonates

• Published in: Green Processing and Synthesis
• Main Authors: Suerbaev, Khakim A., Aldabergenov, Mayliby K., Kudaibergenov, Nurbolat Zh.
• Format: Article in Journal/Newspaper
• Language: unknown
• Published: Walter de Gruyter GmbH 2015
• Subjects: Health, Toxicology and Mutagenesis; Industrial and Manufacturing Engineering; Fuel Technology; Renewable Energy, Sustainability and the Environment; General Chemical Engineering; Environmental Chemistry; Carbonic acid
• Online Access: http://dx.doi.org/10.1515/gps-2014-0098; https://www.degruyter.com/document/doi/10.1515/gps-2014-0098/pdf

Abstract The objective of this work was to investigate the possibility of using alkali metal salts of ethylcarbonic acid as a carboxylating reagent in phenol (naphthols) carboxylation and developing a new and simple method for the synthesis of hydroxybenzoic and hydroxynaphthoic acids having broad practical application. It was found that sodium ethyl carbonate and potassium ethyl carbonate can be successfully used as carboxylating agents in carboxylation of phenol and naphthols. For the first time, the effects of the gaseous medium (air, carbon dioxide, argon), pressure, temperature and reaction time on the proceedings of the carboxylation reactions were examined. Simple and convenient procedures for the syntheses of o- and p-hydroxybenzoic, p-aminosalicylic, 1-hydroxy-2-naphthoic, 1-hydroxy-4-naphthoic and 2-hydroxy-3-naphthoic acids were developed. New efficient technologies for preparation of drugs salicylic acid (antiseptic activity), p-aminosalicylic acid (antituberculous activity) and p-hydroxybenzoic acid (bactericide activity) based on carboxylation reactions of phenol and m-aminophenol with sodium and potassium salts of ethyl carbonic acid were worked out.