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Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives

The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involv...

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Autores principales: Maret, Corentin, David, Nicolas, Pierrot, David, Léonel, Eric, Levacher, Vincent, Brière, Jean-François, Oudeyer, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537669/
https://www.ncbi.nlm.nih.gov/pubmed/37764480
http://dx.doi.org/10.3390/molecules28186704
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author Maret, Corentin
David, Nicolas
Pierrot, David
Léonel, Eric
Levacher, Vincent
Brière, Jean-François
Oudeyer, Sylvain
author_facet Maret, Corentin
David, Nicolas
Pierrot, David
Léonel, Eric
Levacher, Vincent
Brière, Jean-François
Oudeyer, Sylvain
author_sort Maret, Corentin
collection PubMed
description The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involved in several chemical transformations, underlining their potential as versatile intermediates in synthetic chemistry. A mechanism was also proposed based upon a control experiment and cyclic voltammetry (CV) study.
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spelling pubmed-105376692023-09-29 Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives Maret, Corentin David, Nicolas Pierrot, David Léonel, Eric Levacher, Vincent Brière, Jean-François Oudeyer, Sylvain Molecules Article The electrocarboxylation of α,α-dichloroarylmethane derivatives in the presence of CO(2) was achieved, providing several α-chloroarylacetic acid derivatives with modest yields but high selectivity (chlorinated vs. non-chlorinated or dicarboxylic acid products). The obtained products were then involved in several chemical transformations, underlining their potential as versatile intermediates in synthetic chemistry. A mechanism was also proposed based upon a control experiment and cyclic voltammetry (CV) study. MDPI 2023-09-20 /pmc/articles/PMC10537669/ /pubmed/37764480 http://dx.doi.org/10.3390/molecules28186704 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maret, Corentin
David, Nicolas
Pierrot, David
Léonel, Eric
Levacher, Vincent
Brière, Jean-François
Oudeyer, Sylvain
Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title_full Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title_fullStr Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title_full_unstemmed Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title_short Synthesis of α-Chloroarylacetic Acid via Electrochemical Carboxylation of α,α-Dichloroarylmethane Derivatives
title_sort synthesis of α-chloroarylacetic acid via electrochemical carboxylation of α,α-dichloroarylmethane derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537669/
https://www.ncbi.nlm.nih.gov/pubmed/37764480
http://dx.doi.org/10.3390/molecules28186704
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