Steglich esterification
| Steglich esterification | |
|---|---|
| Named after | Wolfgang Steglich | 
| Reaction type | Coupling reaction | 
| Identifiers | |
| Organic Chemistry Portal | steglich-esterification | 
The Steglich esterification is a variation of an esterification with dicyclohexylcarbodiimide as a coupling reagent and 4-dimethylaminopyridine as a catalyst. The reaction was first described by Wolfgang Steglich in 1978. It is an adaptation of an older method for the formation of amides by means of DCC (dicyclohexylcarbodiimide) and 1-hydroxybenzotriazole (HOBT).
This reaction generally takes place at room temperature. A variety of polar aprotic solvents can be used. Because the reaction is mild, esters can be obtained that are inaccessible through other methods for instance esters of the sensitive 2,4-dihydroxybenzoic acid. A characteristic is the formal uptake of water generated in the reaction by DCC, forming the urea compound dicyclohexylurea (DCU).