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Diisobutylaluminum hydride → [4-Bromo-2-(methanesulfonyl)phenyl]methanol

HRID 1406304
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HRID 1406304 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6](OC)=[O:7])=[C:4]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:3]=1.CC(C[AlH]CC(C)C)C>C1COCC1>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([CH2:6][OH:7])=[C:4]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:3]=1
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참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 53393139Methyl 4-bromo-2-(methylsulfonyl)benzoate

생성물 1

HCID 59251623[4-Bromo-2-(methanesulfonyl)phenyl]methanol수율 87.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirring solution of methyl 4-bromo-2-(methylsulfonyl)benzoate (1000 mg, 3.41 mmol) in THF (20 mL) at −78° C. was added DIBAL-H solution (1.0 M in hexanes, 7.50 ml, 2.20 equiv.) dropwise. The mixture was stirred for 15 min and then gradually warmed to room temperature and stirred for another 4 hour. LCMS indicated clean conversion of the starting material to the product. The reaction was quenched with sodium bicarbonate, and then concentrated to dryness. The resulting solids were stirred with DCM (100 ml) for 1 hour and then filtered. The solids were rinsed with EtOAc until the rinse was free of product. The combined filtrate were dried over sodium sulfate, concentrated to dryness to give the desired product (788 mg)

후처리

  1. stirringstirred for another 4 hour
  2. customThe reaction was quenched with sodium bicarbonate
  3. concentrationconcentrated to dryness
  4. stirringThe resulting solids were stirred with DCM (100 ml) for 1 hour
  5. filtrationfiltered
  6. washThe solids were rinsed with EtOAc until the rinse
  7. dry with materialThe combined filtrate were dried over sodium sulfate
  8. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-817cd5d0e2644f67ac271e2eb6962956
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916593B2

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