Also known as: Fischer-Speier esterification
The Fischer esterification is an organic reaction used to convert a carboxylic acid and an alcohol to an ester using an acid catalyst. Formula of 926659-01-0 204715-91-3 uses The mechanism begins with protonation of the carbonyl group of the carboxylic acid, which is then attacked by the alcohol. Proton transfer and the subsequent release of water result in an oxonium ion intermediate. A final deprotonation step provides the ester product. [1]
Mechanism
References:
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Fischer, E.; Speier, A. Ber. Dtsch. Chem. Ges. 1895, 28, 3252–3258.
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