Reacción #1810791

ord-f53083cc4a4d49238dacc84eedf1a2d3

Ecuación de reacción

[Na]
sodium
O=C(O)CCCO
4-hydroxybutyric acid
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
C(=NC1CCCCC1)=NC1CCCCC1
N,N′-dicyclohexylcarbodiimide
COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1
4,4′-dimethoxytrityl chloride
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
desired compound
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
4-Nitrophenyl 4-(4,4′-dimethoxytrityloxy)butyrate

Disolventes

Condiciones de reacción

Temperatura
22°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe precipitated dicyclohexylurea is filtered off
  2. 2
    Lavadowashed with dichloromethane
  3. 3
    ConcentraciónThe filtrate is concentrated
  4. 4
    OtroThe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07485421B2uspto-grants-2009_02