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DCID-mediated esterification of carboxylic acids with alcohols under mild conditions

DCID (Dichloroimidazolidinedione) 2 is used as a novel coupling reagent for the esterification of carboxylic acids with alcohols at room temperature. The reaction represents the first DCID-promoted esterification under mild conditions with good to excellent yields. Reactions can proceed smoothly wit...

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Autores principales: Nasiri, Farzaneh, Mokhtari, Javad, Taheri, Salman, Mirjafary, Zohreh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498154/
https://www.ncbi.nlm.nih.gov/pubmed/37711370
http://dx.doi.org/10.1039/d3ra04048h
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author Nasiri, Farzaneh
Mokhtari, Javad
Taheri, Salman
Mirjafary, Zohreh
author_facet Nasiri, Farzaneh
Mokhtari, Javad
Taheri, Salman
Mirjafary, Zohreh
author_sort Nasiri, Farzaneh
collection PubMed
description DCID (Dichloroimidazolidinedione) 2 is used as a novel coupling reagent for the esterification of carboxylic acids with alcohols at room temperature. The reaction represents the first DCID-promoted esterification under mild conditions with good to excellent yields. Reactions can proceed smoothly with those bearing electron-withdrawing and donating group(s) on the carboxylic acids and benzyl alcohols at ambient temperature. Furthermore, we proposed a plausible mechanism and confirmed it by isolating and characterizing intermediates 3a and 7. The structures of the synthesized compounds were confirmed by comparison of melting points and NMR spectra.
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spelling pubmed-104981542023-09-14 DCID-mediated esterification of carboxylic acids with alcohols under mild conditions Nasiri, Farzaneh Mokhtari, Javad Taheri, Salman Mirjafary, Zohreh RSC Adv Chemistry DCID (Dichloroimidazolidinedione) 2 is used as a novel coupling reagent for the esterification of carboxylic acids with alcohols at room temperature. The reaction represents the first DCID-promoted esterification under mild conditions with good to excellent yields. Reactions can proceed smoothly with those bearing electron-withdrawing and donating group(s) on the carboxylic acids and benzyl alcohols at ambient temperature. Furthermore, we proposed a plausible mechanism and confirmed it by isolating and characterizing intermediates 3a and 7. The structures of the synthesized compounds were confirmed by comparison of melting points and NMR spectra. The Royal Society of Chemistry 2023-09-13 /pmc/articles/PMC10498154/ /pubmed/37711370 http://dx.doi.org/10.1039/d3ra04048h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Nasiri, Farzaneh
Mokhtari, Javad
Taheri, Salman
Mirjafary, Zohreh
DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title_full DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title_fullStr DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title_full_unstemmed DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title_short DCID-mediated esterification of carboxylic acids with alcohols under mild conditions
title_sort dcid-mediated esterification of carboxylic acids with alcohols under mild conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498154/
https://www.ncbi.nlm.nih.gov/pubmed/37711370
http://dx.doi.org/10.1039/d3ra04048h
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AT mokhtarijavad dcidmediatedesterificationofcarboxylicacidswithalcoholsundermildconditions
AT taherisalman dcidmediatedesterificationofcarboxylicacidswithalcoholsundermildconditions
AT mirjafaryzohreh dcidmediatedesterificationofcarboxylicacidswithalcoholsundermildconditions