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Methanol → 4-Bromo-3-(hydroxymethyl)-2-propylphenol

HRID 552445
ノート
印刷プレビュー

反応式

HRID 552445 の反応式
[OH:1][CH2:2][C:3]1[C:4]([CH2:10][CH2:11][CH3:12])=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1.CO.[Br-:15].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC>ClCCl>[Br:15][C:8]1[CH:7]=[CH:6][C:5]([OH:9])=[C:4]([CH2:10][CH2:11][CH3:12])[C:3]=1[CH2:2][OH:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 23500184Tetra-n-butylammonium tribromideHCID 579008323-(Hydroxymethyl)-2-propylphenol

生成物 1

HCID 579008284-Bromo-3-(hydroxymethyl)-2-propylphenol収率 67.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 3-(hydroxymethyl)-2-propylphenol (1.05 g, 6.32 mmol) in dichloromethane (50 mL)-methanol (30 mL) mixtures, tetrabutylammonium tribromide (3.20 g, 6.64 mmol) was added at 0° C. The mixture was stirred at the same temperature for 1 hour. Solvent was evaporated under reduced pressure. The residue was added with water and extracted with ethyl acetate. Subsequently, the organic layer was washed with saturated saline, dried using anhydrous sodium sulfate, and concentrated in vacuum. The obtained residue was purified using silica-gel column chromatography (hexane/ethyl acetate) and the title compound (1.04 g, 67%) was obtained as colorless crystalline powder.

後処理

  1. customSolvent was evaporated under reduced pressure
  2. additionThe residue was added with water
  3. extractionextracted with ethyl acetate
  4. washSubsequently, the organic layer was washed with saturated saline
  5. customdried
  6. concentrationconcentrated in vacuum
  7. customThe obtained residue was purified

出典と根拠

ORDレコード
ord-36010b1af34249a0a4a818c1044ab1d7
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07951822B2

反応ノート

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