Dichloromethane → methyl (2R, 3S)-2-(N-benzoylamino)methyl-3-hydroxybutanoate

HRID 703279

반응식

HRID 703279 반응식
C(Cl)Cl.[C:4]([NH:12][CH2:13][CH:14]([C:19](=[O:21])[CH3:20])[C:15]([O:17][CH3:18])=[O:16])(=[O:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>CCN(CC)CC>[C:4]([NH:12][CH2:13][C@H:14]([C@@H:19]([OH:21])[CH3:20])[C:15]([O:17][CH3:18])=[O:16])(=[O:11])[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1

참가 물질

4

반응물 2

HCID 6344DichloromethaneHCID 11831808Methyl 2-((benzoylamino)methyl)-3-oxobutanoate

생성물 1

HCID 10264162methyl (2R, 3S)-2-(N-benzoylamino)methyl-3-hydroxybutanoate수율 91%

시약·촉매·용매 1

HCID 8471Triethylamine용매

반응 조건

온도
45 °C

실험 절차

In a 100 ml-volume autoclave whose atmosphere had been displaced with nitrogen was added a methylene chloride solution of 2.5 g of methyl 2-(N-benzoylamino)methyl-3-oxobutanoate and 84.5 mg (0.05 mmole) of Ru2Cl4 ((-)-BINAP2 (NEt3), and a reaction was conducted by stirring at 45° C. under a hydrogen pressure of 70 kg/cm2 for 24 hours. The reaction mixture was taken out, and the solvent was removed by distillation under reduced pressure of 20 mmHg at 30° C. The residue was purified by silica gel column chromatography using a 7/3 (by volume) mixture of hexane and isopropanol as an eluent to obtain 2.27 g (yield: 91%) of methyl (2R, 3S)-2-(N-benzoylamino)methyl-3-hydroxybutanoate having an optical purity of 97 %ee.

후처리

  1. customthe solvent was removed by distillation under reduced pressure of 20 mmHg at 30° C
  2. customThe residue was purified by silica gel column chromatography
  3. additiona 7/3 (by volume) mixture of hexane and isopropanol as an eluent

출처 및 근거

ORD 기록
ord-40ea430dc7dc49dbb7f8848a2d950e32
출처 데이터셋
uspto-grants-1991_01
특허 번호
US04981992

연결된 노트

불러오는 중…