Réaction #1810791

ord-f53083cc4a4d49238dacc84eedf1a2d3

Solvants

Conditions de réaction

Température
22°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe precipitated dicyclohexylurea is filtered off
  2. 2
    Lavagewashed with dichloromethane
  3. 3
    ConcentrationThe filtrate is concentrated
  4. 4
    AutreThe residue is purified on a silica gel column (10-50% ethyl acetate and 1% triethylamine in petroleum ether)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07485421B2uspto-grants-2009_02