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

HRID 238943ノート

反応式

HRID 238943 の反応式
[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]

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8f6474ba20e846e49214da9fa1a069b8
出典データセット
uspto-grants-2014_02
特許番号
US08642640B2

反応ノート

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