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Boron tribromide → 5-Bromo-2-(1-hydroxy-2-methylpropan-2-yl)phenol

HRID 1054866
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HRID 1054866 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:12])([CH3:11])[CH2:9][OH:10])=[C:4]([O:13]C)[CH:3]=1.B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:12])([CH3:11])[CH2:9][OH:10])=[C:4]([OH:13])[CH:3]=1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 866987222-(4-Bromo-2-methoxyphenyl)-2-methylpropan-1-ol

생성물 1

HCID 866988495-Bromo-2-(1-hydroxy-2-methylpropan-2-yl)phenol수율 32%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2-(4-bromo-2-methoxyphenyl)-2-methylpropan-1-ol (300 mg, 1.16 mmol) in dichloromethane (5 mL) was added dropwise boron tribromide (580 mg, 2.32 mmol) at −78° C. under nitrogen. The reaction mixture was warmed to room temperature and stirred for 30 minutes. The reaction was quenched with water (10 mL) and extracted with dichloromethane (20 mL). The organic layer was washed with aq. sodium bicaronate (20 mL), brine (20 mL), dried over sodium sulfate, filtered and concentrated to give a crude residue, which was purified by flash chromatography to give the title compound (90 mg, 32%) as a white solid.

후처리

  1. customThe reaction was quenched with water (10 mL)
  2. extractionextracted with dichloromethane (20 mL)
  3. washThe organic layer was washed with aq. sodium
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give a crude residue, which
  8. customwas purified by flash chromatography

출처 및 근거

ORD 기록
ord-395146972f36469a85edfa39b4a33a25
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394285B2

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