Water → 4-Amino-1-(phenylmethyl)-3-pyrrolidinemethanol

HRID 1461040노트

반응식

HRID 1461040 반응식
[CH2:1]([N:8]1[CH2:12][C:11](=[N:13]O)[CH:10]([C:15](OCC)=[O:16])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].COCCO[Al+]OCCOC.[Na+].[H-].O>C1(C)C=CC=CC=1>[NH2:13][CH:11]1[CH:10]([CH2:15][OH:16])[CH2:9][N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:12]1

참가 물질

5

반응물 3

HCID 962WaterHCID 21584525Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 86745294HCID 86745294, 화합물

생성물 1

HCID 150238514-Amino-1-(phenylmethyl)-3-pyrrolidinemethanol수율 52.4%

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A solution of 5.24 g (0.02 mole) of 1-benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine [prepared as described in step (a) above] in 10 ml of toluene was added dropwise to 28 ml of a 3.4M solution of sodium bis(2-methoxyethoxy)aluminum hydride in toluene over a period of 1 hour. The mixture was stirred at room temperature for 1.5 hours and was then heated under reflux for 2 hours. At the end of this time, the reaction mixture was allowed to cool to room temperature, after which ice and water were added to it to form a precipitate, which was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using methanol as the eluent, to afford 2.16 g of 3-amino-1-benzyl-4-hydroxymethylpyrrolidine as a brown oil.

후처리

  1. temperaturewas then heated
  2. temperatureunder reflux for 2 hours
  3. temperatureto cool to room temperature
  4. customto form a precipitate, which
  5. customwas removed by filtration
  6. concentrationThe filtrate was concentrated by evaporation under reduced pressure
  7. customthe residue was purified by column chromatography through silica gel

출처 및 근거

ORD 기록
ord-b5f87915d4264702ad96cfbe44266631
출처 데이터셋
uspto-grants-1991_12
특허 번호
US05073556

반응 노트

불러오는 중…