Reaktion #8554

ord-4b3497d821714899838080df19bf8f51

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAt room temperature
  2. 2
    Sonstigethe liquid reaction mixture
  3. 3
    Extraktionfollowed by extraction with ethyl acetate
  4. 4
    WaschenThe organic layer was washed with water
  5. 5
    Trocknena saturated aqueous solution of ammonium chloride and dried over anhydrous magnesium sulfate
  6. 6
    SonstigeAfter evaporating the solvent

Vorschrift

At room temperature, sodium borohydride (35.7 mg) was suspended in chlorobenzene (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in chlorobenzene was added to the solution. After adding methanol (137.4 mg), the liquid reaction mixture was stirred for 6 hours. Then water was added to the liquid reaction mixture followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of ammonium chloride and dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography to thereby give 162.9 mg (99.8% ee) of the title compound as an oily substance. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 51.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087778B2uspto-grants-2006_08