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Highly efficient esterification of carboxylic acids with O-H nucleophiles through acid/iodide cooperative catalysis.

Authors :
Zuo D
Xiao X
Ma X
Nie P
Liu L
Chen T
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2024 Jul 31; Vol. 22 (30), pp. 6181-6188. Date of Electronic Publication: 2024 Jul 31.
Publication Year :
2024

Abstract

The esterification of carboxylic acids is an important reaction for preparing esters which find wide applications in various research fields. In this manuscript, we report an acid/iodide cooperative catalytic method which enables highly efficient esterification of carboxylic acids with a wide range of equivalent O-H nucleophiles including both alcohols and weak nucleophilic phenols. Under the reaction conditions, both aromatic and aliphatic carboxylic acids including those bearing functional groups work well, furnishing the corresponding esters in good to high yields. Moreover, this reaction is scalable and applicable to the modification of bioactive molecules. These results demonstrate the synthetic value of this new reaction in organic synthesis.

Details

Language :
English
ISSN :
1477-0539
Volume :
22
Issue :
30
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
39016558
Full Text :
https://doi.org/10.1039/d4ob00910j