Reacción #1810791
ord-f53083cc4a4d49238dacc84eedf1a2d3
Ecuación de reacción
sodium
4-hydroxybutyric acid
4-nitrophenol
N,N′-dicyclohexylcarbodiimide
4,4′-dimethoxytrityl chloride
→
desired compound
4-Nitrophenyl 4-(4,4′-dimethoxytrityloxy)butyrate
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
22°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1FiltraciónThe precipitated dicyclohexylurea is filtered off
- 2Lavadowashed with dichloromethane
- 3ConcentraciónThe filtrate is concentrated
- 4OtroThe residue is purified on a silica gel column (10-50% ethyl acetate and 1% triethylamine in petroleum ether)
Procedimiento
The sodium salt of 4-hydroxybutyric acid (1.26 g; 10 mmol) is dissolved in anhydrous pyridine (30 ml), and 4,4′-dimethoxytrityl chloride (3.39 g; 3.05 mmol) is added. After 16 hours, 4-nitrophenol (1.39 g; 10 mmol) and N,N′-dicyclohexylcarbodiimide (2.06 g; 10 mmol) are added, and the mixture is stirred at 22° C. for a further 48 hours. The precipitated dicyclohexylurea is filtered off and washed with dichloromethane. The filtrate is concentrated and the resulting residue is coevaporated twice with toluene. The residue is purified on a silica gel column (10-50% ethyl acetate and 1% triethylamine in petroleum ether). The desired compound is obtained in the form of a pale yellowish-colored oil.