Réaction #1909791

ord-629b7224b37c4aacbd88982eeb240429

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe mixture was extracted with ethyl acetate
  2. 2
    LavageThe organic layer was washed successively with a 10 % aqueous citric acid solution, water
  3. 3
    Séchagea saturated aqueous sodium hydrogen-carbonate solution, water and saturated brine, dried over magnesium sodium sulfate
  4. 4
    Concentrationconcentrated under reduced pressure

Mode opératoire

To a solution of 4-(4-hydroxyphenyl)benzoic acid (3.0 g) and L-phenylalanine ethyl ester hydrochloride (3.38 g) in DMF (30 ml) were added WSC.HCl (2.7 g), HOBT (1.89 g) and triethylamine (2 ml), and the mixture was stirred at room temperature for 14 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with a 10 % aqueous citric acid solution, water, a saturated aqueous sodium hydrogen-carbonate solution, water and saturated brine, dried over magnesium sodium sulfate, and concentrated under reduced pressure to give a crude product of the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE039088E1uspto-grants-2006_05