Esterification is the general name for a chemical reaction in that an ester is the reaction product.
Esterification reactions include
- the reaction of a carboxylic acid halogenide (which is also called acyl halide) with an alcohol/phenole
- the reaction of an alkali carboxylate and an alcohol
H3C-COOH + HO-CH2-CH3 + H2SO4 ----> H3C-COO-CH2-CH3 + H2SO4 + H-0-H
This reaction is the so called tutorial model reaction, which is found in every college-grade tutorial. It is evident and very easy to understand the mechanism of the SN2 (two-phase-nucleophile-substitution) reaction. This reaction works only for special esters and needs much laboratorial skill, because you have to reflux, but to eflux the water, hence the water would lead the reaction to the left side. Besides that, the acidification catalyses the esterification, but in bigger amounts also the hydrolysis. Therefore, it is NOT useful to use sulfuric-acid in doses capable to bind the resulting water.
H3C-COCl + HO-CH2-CH3 ----> H3C-COO-CH2-CH3 + H-Cl
This reaction is NOT a tutorial reaction, hence it is not very evident. But this reaction is easy to perform, even with basic laboratorial skill.
H3C-CO-O-CO-CH3 + HO-CH2-CH3 ----> H3C-COO-CH2-CH3 + H3C-COOH
This reaction is the easiest to perform, although it is rarely cited in tuturials. The reaction has a bigger practical interest: The synthesis of aspirine is performed that way.
H3C-COO- Na+ + HO-CH2-CH3 + H+ ----> H3C-COO-CH2-CH3 + H-0-H
Hence, the reaction runs with sodium acetate in excess, and because sodium acetate binds 3 water molecules, this reaction, I read only once might be possible to be performed.
Last updated: 10-19-2005 21:44:47