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Bromine → 2-Bromo-3,5-difluorophenol

HRID 1815832
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HRID 1815832 반응식
[F:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([F:8])[CH:7]=1.[Br:10]Br>C(=S)=S.C(OCC)C>[Br:10][C:3]1[C:2]([F:1])=[CH:7][C:6]([F:8])=[CH:5][C:4]=1[OH:9]
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참가 물질

5

반응물 2

HCID 24408BromineHCID 759283,5-Difluorophenol

생성물 1

HCID 221448602-Bromo-3,5-difluorophenol수율 60%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 6348Carbon Disulfide용매2회

실험 절차

A solution of 2.6 gm (20 mMol) 3,5-difluorophenol in 20 mL carbon disulfide was cooled to 0° C. and then a solution of 1.02 mL (20 mMol) bromine in 10 mL carbon disulfide was added dropwise over 30 minutes. After stirring for an additional 30 minutes, the reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was diluted with 200 mL diethyl ether and was washed sequentially with aqueous sodium metabisulfite and saturated aqueous sodium chloride. The organic phase was then dried over sodium sulfate and concentrated under reduced pressure. The residue was vacuum distilled to provide 2.5 gm (60%) of 2-bromo-3,5-difluorophenol (b.p.=65° C. (5 mm Hg)).

후처리

  1. stirringstirred for 1.5 hours
  2. washwas washed sequentially with aqueous sodium metabisulfite and saturated aqueous sodium chloride
  3. dry with materialThe organic phase was then dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. distillationdistilled

출처 및 근거

ORD 기록
ord-c40255f429134ed694c52d15f97a4f9c
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06881733B1

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