Réaction #1898866

ord-155cb3f13f074bb9b802ff3ee62ae07e

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ExtractionThe aqueous layer was extracted with EtOAc
  2. 2
    SéchageThe organic layers were dried over MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    Concentrationconcentrated under reduced pressure

Mode opératoire

D-Phenylglycine (R) (85.2 mmol) was dissolved in anhydrous THF (260 mL) with NaHCO3 (256 mmol) in water (260 mL). Ethylchloroformate (0.235 mol) was added. After stirred at room temperature overnight, the reaction mixture was acidified to pH 3 with 1N HCl. The aqueous layer was extracted with EtOAc. The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure to give (R)-2-(ethoxycarbonylamino)-2-phenylacetic acid 41 as a white solid in 82% yield. MS (ESI, EI+) m/z=224.2 (MH+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08362068B2uspto-grants-2013_01