Production of Esters by Reacting Alcohols With Acyl Chlorides
Esters are organic compounds with an -COR functional group
They have characteristic smells and are used in perfumes, cosmetics and as solvents
Esters can be prepared from the condensation reaction between alcohols and carboxylic acids
This is also called an esterification reaction
A more effective way of preparing esters is from the condensation reaction between alcohols and acyl chlorides instead
Unlike the reactions with carboxylic acids, acyl chlorides are more reactive (so the reactions happen faster) and their reactions go to completion (so no equilibrium mixture is formed and the yield of the ester is maximum)
Examples of esterification reactions include:
Formation of ethyl ethanoate from ethanol and ethanoyl chloride
Formation of phenyl benzoate from phenol and benzoyl chloride
Formation of esters from the reaction of alcohols with acyl chlorides