Hydrogen Peroxide → (2R)-2-(4-methoxyphenyl)propanoic acid

HRID 2176879노트

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HRID 2176879 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]([CH3:25])[C:10](N2[C@@H](CC3C=CC=CC=3)COC2=O)=[O:11])=[CH:5][CH:4]=1.[OH-:26].[Li+].OO>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C@@H:9]([CH3:25])[C:10]([OH:11])=[O:26])=[CH:7][CH:8]=1

참가 물질

5

실험 절차

A solution of (S)-3-((R)-2-(4-methoxyphenyl)propanoyl)-4-benzyloxazolidin-2-one (1.50 g, 4.42 mmol) in THF (20 ml) was added to a mixture of lithium hydroxide (750 mg, 17.6 mmol) and hydrogen peroxide (0.9 ml, 26.5 mmol, 30% in water). The reaction mixture was stirred at room temperature for 3 h. Then the solvent was evaporated, the residue was acidified with diluted HCl (10 ml) and extracted with DCM (3×50 ml). The combined organic layers was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude compound was purified by column chromatography over silica gel (60-120 mesh) using ethyl acetate (20%) in petroleum ether as eluent to afford 600 mg (76%) of (R)-2-(4-methoxyphenyl)propanoic acid as colorless liquid.

후처리

  1. customThen the solvent was evaporated
  2. extractionextracted with DCM (3×50 ml)
  3. dry with materialThe combined organic layers was dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe crude compound was purified by column chromatography over silica gel (60-120 mesh)

출처 및 근거

ORD 기록
ord-d6e1c387899b4049b0d52e8561981e67
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09067888B2

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