Boron trifluoride etherate → (2S, 4S)-2-Hydroxymethyl-4-hydroxy-1-(4-toluenesulfonyl) pyrrolidine

HRID 1087625노트

반응식

HRID 1087625 반응식
[BH4-].[Na+].B(F)(F)F.CCOCC.[C:12]1([CH3:30])[CH:17]=[CH:16][C:15]([S:18]([N:21]2[CH2:28][CH:27]([OH:29])[CH2:26][C@@H:22]2[C:23](O)=[O:24])(=[O:20])=[O:19])=[CH:14][CH:13]=1>C1COCC1>[OH:24][CH2:23][C@@H:22]1[CH2:26][C@H:27]([OH:29])[CH2:28][N:21]1[S:18]([C:15]1[CH:16]=[CH:17][C:12]([CH3:30])=[CH:13][CH:14]=1)(=[O:20])=[O:19]

참가 물질

5

실험 절차

4.14 g (109.5 mmol) of sodium borohydride was suspended in 150 ml of THF at 0° C. and 17.6 ml (142.2 mmol) of borontrifluoride etherate was added dropwise over a period of 10 minutes. 15.6 g (54.7 mmol) of 1-(4-toluenesulfonyl)-4-hydroxy-D-proline was added in portions and the mixture was allowed to stir at room temperature for 16 hours. The reaction was then cooled to 0° C. and quenched with methanol: 10% aqueous HC1 solution was then added and the mixture was gently heated to 60° C. for 1 hour. The pH of the reaction was adjusted to neutral with 50% aqueous sodium hydroxide solution and the volatiles were evaporated under reduced pressure. The product was then isolated via filtration and the filter cake was washed with water. Drying under vacuum at 60° C. for 12 hours yielded 10.2 g of the product as a white solid in 69% yield. M.P.=103°-105° C.

후처리

  1. temperatureThe reaction was then cooled to 0° C.
  2. customquenched with methanol
  3. addition10% aqueous HC1 solution was then added
  4. temperaturethe mixture was gently heated to 60° C. for 1 hour
  5. customthe volatiles were evaporated under reduced pressure
  6. customThe product was then isolated via filtration
  7. washthe filter cake was washed with water
  8. customDrying under vacuum at 60° C. for 12 hours

출처 및 근거

ORD 기록
ord-779b8fe6f65b4d25863377be86fda247
출처 데이터셋
uspto-grants-1991_07
특허 번호
US05036153

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