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

HRID 1054866
ノート
印刷プレビュー

反応式

HRID 1054866 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-395146972f36469a85edfa39b4a33a25
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09394285B2

反応ノート

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