Benzoyl chloride → (S)-beta-Benzoyloxy-gamma-butyrolactone

HRID 657481

반응식

HRID 657481 반응식
[OH:1][C@@H:2]1[CH2:7][O:6][C:4](=[O:5])[CH2:3]1.[C:8](Cl)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9]>N1C=CC=CC=1>[C:8]([O:1][C@@H:2]1[CH2:7][O:6][C:4](=[O:5])[CH2:3]1)(=[O:9])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

참가 물질

4

실험 절차

To the solution of (S)-β-Hydroxy-γ-butyrolactone (1.0 g, 9.8 mmol) in 25 mL pyridine was added dropwise BzCl (1.4 mL, 12.2 mmol) at 0° C. The reaction mixture was warmed to room temperature and stirred overnight. The reaction was concentrated and coevaporated with toluene two times in vacuo. The residue was partitioned between H2O (15 mL) and EtOAc (40 mL). The organic layer was washed with water and brine, and concentrated in vacuo. The residue was purified by chromatography on a silica gel column (n-hexane/EtOAc=8:1) to afford 101 (1.78 g, 8.6 mmol) as a white solid, in 89% yield, which was characterized as follows:

후처리

  1. concentrationThe reaction was concentrated
  2. customThe residue was partitioned between H2O (15 mL) and EtOAc (40 mL)
  3. washThe organic layer was washed with water and brine
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by chromatography on a silica gel column (n-hexane/EtOAc=8:1)

출처 및 근거

ORD 기록
ord-7e29da1f29b94645bdad163192ea4989
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08076310B2

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