Moore, James Alexander Formerly, Department of Chemistry, University of Delaware, Newark, Delaware.
Last reviewed:August 2019
- Carbon acylation
- Other carboxyl activation methods
- Related Primary Literature
- Additional Reading
A process in which a hydrogen atom in an organic compound is replaced by an acyl group (RCO where R = an organic group). The reaction involves substitution by a nucleophile (electron donor) at the electrophilic carbonyl group (CO) of a carboxylic acid derivative. The substitution usually proceeds by an addition-elimination sequence [reaction]. Two common reagents, with the general formula RCOX, that bring about acylation are acid halides (X = Cl,Br) and anhydrides (X = OCOR). There are also other acylating reagents. The carboxylic acid (X = OH) itself can function as an acylating agent when it is protonated by a strong acid catalyst as in the direct esterification of an alcohol. Typical nucleophiles in the acylation reaction are alcohols (ROH) or phenols (ArOH), both of which give rise to esters, and ammonia or amines (RNH2), which give amides. See also: Acid anhydride; Acid halide; Amide; Amine; Electrophilic and nucleophilic reagents
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