EventsThe 25th International Electronic Conference on Synthetic Organic Chemistry
Published
with-doi10.3390/ecsoc-25-11693 (registering DOI)
This submission belongs to the session S1. General Organic Synthesis of the event The 25th International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2021
Academic Editor
author-avatarJulio A. Seijas
Citation
Alfiya R Bayguzina, Ilfir R Ramazanov, Iron-catalyzed synthesis of alkyl esters of benzoic acid from benzene and its derivatives with use of CCl₄ – alcohol reagent system, in Proceedings of The 25th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2021, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-25-11693
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Iron-catalyzed synthesis of alkyl esters of benzoic acid from benzene and its derivatives with use of CCl4 – alcohol reagent system

1. Institute of Petrochemistry and Catalysis of Russian Academy of Sciences
2. Ufa State Petroleum Technological University
Abstract

The aim of this work is to develop a one-stage catalytic method for the preparation of alkyl esters of benzoic acid by the direct reaction of benzene and its derivatives with alcohols and halogenmethanes. We found that the reaction of benzene, phenol, and anisole with CCl4 and alcohol under the action of the [Fe] –acetylacetone catalyst leads to the formation of practically important esters of alkyl benzoates, as well as salicylic and p-hydroxybenzoic acids. The advantage of the developed method for the synthesis of esters of benzoic acid is the availability and low cost of the main starting reagents - benzene, phenol, anisole, CCl4, alcohols and iron, cost reduction and simplification of technology, moderate reaction time (6 h), relatively low temperature, one-step process, possibility the use of this reaction in an industrial environment (scaling).

Keywords
benzene
phenol
anisole
esters of carboxylic acids
catalysis
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