Knoevenagel Reaction

Knoevenagel reaction

[kə′nē·və‚näg·əl rē‚ak·shən] (organic chemistry) The condensation of aldehydes with compounds containing an activated methylene (=CH2) group.

Knoevenagel Reaction

 

the condensation of aldehydes or ketones with compounds containing an active methylene group in the presence of bases, resulting in the formation of ethylene derivatives. For example, a derivative of cinnamic acid (III) is obtained during the condensation of benzaldehyde (I) with the diethyl ester of malonic acid (II) in the presence of piperidine:

The Knoevenagel reaction is widely used in the laboratory for organic synthesis and in the chemical-pharmaceutical and perfume industries. The German scientist E. Knoevenagel discovered the reaction in 1896.

REFERENCE

Surrey, A. Spravochnik po organicheskim reaktsiiam. Moscow, 1962. (Translated from English.)