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4-Isopropylresorcinol → 4-Bromo-6-(propan-2-YL)benzene-1,3-diol

HRID 1947172
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반응식

HRID 1947172 반응식
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][C:5]=1[OH:11])([CH3:3])[CH3:2].[Br-:12].[Br-].[Br-].C([N+](C)(C)C)C1C=CC=CC=1.C([N+](C)(C)C)C1C=CC=CC=1.C([N+](C)(C)C)C1C=CC=CC=1>C(Cl)Cl>[Br:12][C:8]1[CH:9]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5]([OH:11])=[CH:6][C:7]=1[OH:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 901354-IsopropylresorcinolHCID 53442637Benzyltrimethylammoniumtribromide

생성물 1

HCID 598299224-Bromo-6-(propan-2-YL)benzene-1,3-diol수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-isopropyl-benzene-1,3-diol (IMO-a: 9.13 g, 60 mmol) and benzyltrimethyl ammoniumtribromide (24.6 g, 63 mmol) and methylene chloride 250 mL were placed in a 500 mL three-neck flask and were stirred at room temperature for 4 hours. After the reaction was finished, the reaction mixture was washed twice with saturated ammonium chloride and once with saturated sodium chloride, and then dried over anhydrous sodium sulfate. After filtration and evaporation, the residue was purified by silica gel column chromatography to obtain the title compound (IM1-a: 10.5 g, 76%).

후처리

  1. washthe reaction mixture was washed twice with saturated ammonium chloride and once with saturated sodium chloride
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationAfter filtration and evaporation
  4. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-50990841d12049e8b3139ef576e9433b
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399464B2

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