تفاعل #8543

ord-cefec37d8b7542628f3b9646541dcee4

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat room temperature
  2. 2
    أخرىThe liquid reaction mixture
  3. 3
    درجة الحرارةwas heated
  4. 4
    درجة الحرارةunder reflux for 6 hours
  5. 5
    أخرىthe solvent was evaporated
  6. 6
    workup.ADDITIONTo the obtained residue was added chloroform (10 ml)
  7. 7
    غسيلNext, the organic layer was washed with a saturated aqueous solution of sodium chloride and water
  8. 8
    تجفيفdried over anhydrous magnesium sulfate
  9. 9
    أخرىAfter evaporating the solvent

الإجراء التجريبي

(2R)-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 (10 ml). 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 (245 mg) as a pale yellow oily substance. The optical purity of the product was 98% ee. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 7.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087778B2uspto-grants-2006_08