반응 #8542
ord-6c010bf21eb44d308a098365cac4795c
반응 방정식
반응 조건
후처리
- 1기타at room temperature
- 2기타The liquid reaction mixture
- 3온도was heated
- 4온도under reflux for 6 hours
- 5기타the solvent was evaporated
- 6workup.ADDITIONTo the obtained residue was added chloroform
- 7세척Next, the organic layer was washed with a saturated aqueous solution of sodium chloride and water
- 8건조dried over anhydrous magnesium sulfate
- 9기타After 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.