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

HRID 552445
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HRID 552445 반응식
[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]
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참가 물질

5

반응물 3

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

생성물 1

HCID 579008284-Bromo-3-(hydroxymethyl)-2-propylphenol수율 67.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-36010b1af34249a0a4a818c1044ab1d7
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07951822B2

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