Benzyl 2,2,2-trichloroacetimidate → (3S)-3-(benzyloxy)butanoic acid ethyl ester

HRID 238943노트

반응식

HRID 238943 반응식
[CH2:1]([O:3][C:4](=[O:9])[CH2:5][C@@H:6]([OH:8])[CH3:7])[CH3:2].ClC(Cl)(Cl)C(=N)O[CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(Cl)Cl.FC(F)(F)S(O)(=O)=O>[CH2:1]([O:3][C:4](=[O:9])[CH2:5][C@@H:6]([O:8][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH3:7])[CH3:2]

참가 물질

5

실험 절차

Under a nitrogen atmosphere, to a solution of (S)-(+)-3-hydroxybutyric acid ethyl ester (100 g, 0.76 mol) in methylene chloride (1.0 L), benzyl 2,2,2-trichloroacetoimidate (381 g, 1.5 mol) and trifluoromethanesulfonic acid (6.7 mL, 76 mmol) were gradually added, and the mixture was stirred at room temperature overnight. The precipitated solid was filtered, and after the mother liquid was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, it was dried with sodium sulfate and the solvent was distilled off under reduced pressure. Hexane was added to the residue, and after the solid was filtered again, the solvent of the mother liquid was distilled off under reduced pressure to give (3S)-3-(benzyloxy)butanoic acid ethyl ester (339 g) as a mixture. The present compound was used for the subsequent reaction without further purification.

후처리

  1. filtrationThe precipitated solid was filtered
  2. washafter the mother liquid was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, it
  3. dry with materialwas dried with sodium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. additionHexane was added to the residue
  6. filtrationafter the solid was filtered again
  7. distillationthe solvent of the mother liquid was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-8f6474ba20e846e49214da9fa1a069b8
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642640B2

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