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2,6-Dimethoxyphenol → 3-Bromo-2,6-dimethoxyphenol

HRID 2171140
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HRID 2171140 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[OH:11].[Br:12]Br>C(Cl)(Cl)(Cl)Cl>[Br:12][C:8]1[C:3]([O:2][CH3:1])=[C:4]([OH:11])[C:5]([O:9][CH3:10])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 70412,6-DimethoxyphenolHCID 24408Bromine

생성물 1

HCID 150736683-Bromo-2,6-dimethoxyphenol수율 66.1%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매2회

실험 절차

To a stirring solution of 2,6-dimethoxy-phenol (2 g, 12.98 mmol) in CCl4 (70 mL) at −10° C. was added bromine (2.07 g, 12.98 mmol) and stirred for 2 h. The reaction mixture was diluted with CCl4, washed with water and the combined CCl4 layers were washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford 3-Bromo-2,6-dimethoxy-phenol as a solid (2 g, 66%).

후처리

  1. washwashed with water
  2. washthe combined CCl4 layers were washed with brine
  3. dry with materialdried over anhydrous sodium sulphate
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7e438f28456f4df9b63781dbf318c234
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051290B2

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