반응 #8542

ord-6c010bf21eb44d308a098365cac4795c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at room temperature
  2. 2
    기타The liquid reaction mixture
  3. 3
    온도was heated
  4. 4
    온도under reflux for 6 hours
  5. 5
    기타the solvent was evaporated
  6. 6
    workup.ADDITIONTo the obtained residue was added chloroform
  7. 7
    세척Next, the organic layer was washed with a saturated aqueous solution of sodium chloride and water
  8. 8
    건조dried over anhydrous magnesium sulfate
  9. 9
    기타After evaporating the solvent

실험 절차

(2S)-2-(2,3,4-trifluoroanilino)propionic acid (219 mg; 99% ee) was dissolved in ethanol (2 ml) and hydrochloric acid (5 mol/l; 0.2 ml) was added thereto at room temperature. The liquid reaction mixture was heated under reflux for 6 hours and then the solvent was evaporated. To the obtained residue was added chloroform. Next, the organic layer was washed with a saturated aqueous solution of sodium chloride and water and dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography (ethyl acetate-normal hexane=1:4) to give the title compound (246 mg) as a pale yellow oily substance. The optical purity of the product was 99% ee. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 7.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087778B2uspto-grants-2006_08