Benzaldehyde → methyl (2R)-2-(benzylamino)propanoate

HRID 264295

반응식

HRID 264295 반응식
Cl.[CH3:2][O:3][C:4](=[O:8])[C@@H:5]([CH3:7])[NH2:6].[CH:9](=O)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C([BH3-])#N.[Na+]>CO>[CH3:2][O:3][C:4](=[O:8])[C@@H:5]([CH3:7])[NH:6][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

참가 물질

5

실험 절차

To a solution of D-alanine methyl ester hydrochloride (3.0 g, 21.5 mmol) in methanol (10 mL) is added benzaldehyde (2.3 mL, 22.6 mmol). The reaction mixture is stirred at room temperature for 3 hours. The solvent is then evaporated. To the resultant residue is added acetic acid (15 mL) and methanol (1 mL) followed by portionwise addition of sodium cyanoborohydride (1.35 g, 21.5 mmol) at room temperature. The mixture is stirred overnight, and then the solvent is evaporated. The remaining residue is diluted with water (75 mL) and basified with Na2CO3. The mixture is extracted with ethyl acetate (3×75 mL). The combined organic extracts are washed with brine (50 mL), dried (Na2SO4), and the solvent is evaporated to give N-benzyl-D-alanine methyl ester.

후처리

  1. customThe solvent is then evaporated
  2. additionTo the resultant residue is added acetic acid (15 mL) and methanol (1 mL)
  3. stirringThe mixture is stirred overnight
  4. customthe solvent is evaporated
  5. additionThe remaining residue is diluted with water (75 mL)
  6. extractionThe mixture is extracted with ethyl acetate (3×75 mL)
  7. washThe combined organic extracts are washed with brine (50 mL)
  8. dry with materialdried (Na2SO4)
  9. customthe solvent is evaporated

출처 및 근거

ORD 기록
ord-1e2135e7b33748c5989125d07bdcebe3
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05646167

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