Online Chemistry notes

Claisen condensation reaction – Examples and Mechanism

Claisen condensation reaction


Condensation between two molecules of esters having α-hydrogen atom in the presence of strong base like sodium ethoxide and an acid to form β-keto ester is known as Claisen condensation reaction. Eg.


Mechanism of Claisen condensation reaction


Taking ethyl acetate (ethyl ethanoate) as an example, Claisen condensation reaction involves following steps:

Step-I: In this step, ethoxide ion removes a proton from α-carbon of one molecule of ethyl acetate to form a carbocation.

Step-II: In this step, the carbanion (i.e. nucleophile) attacks the carbonyl carbon of second ester molecule to displace ethoxide ion and forms the keto ester.

Step-III: In this step, there is an acid base reaction between ethoxide ion and β-keto ester to give β-keto ester anion and ethanol.

Step-IV: In this step, an acid is added to the reaction mixture which gives proton to the β-keto ester anion to form the β-keto ester which is in equilibrium with its enol form.

Note:

Keto-enol tautomerism :

Keto-enol tautomerism is a special type of isomerism in which two isomeric forms, keto and enol exist in dynamic equilibrium with each other. There is transfer of a α- hydrogen to the oxygen atom of carbonyl group and vice-versa.


References