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Hydrogen Bromide → 3-Bromo-5-iodophenol

HRID 1784829
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HRID 1784829 반응식
[Br:1][C:2]1[CH:7]=[C:6]([O:8]C)[CH:5]=[C:4]([I:10])[CH:3]=1.Br>C(O)(=O)C.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[Br:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([I:10])[CH:3]=1
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참가 물질

5

반응물 2

HCID 260Hydrogen BromideHCID 509981531-Bromo-3-iodo-5-methoxybenzene

생성물 1

HCID 226301823-Bromo-5-iodophenol수율 352.9%

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 176Acetic Acid용매

실험 절차

1-Bromo-3-iodo-5-methoxy-benzene (6.29 g, 20.1 mmol) was suspended in a solution of hydrogen bromide in acetic acid (33%, 150 mL). Tetrabutylammonium bromide (0.5 g, 1.55 mmol) was added and the mixture was heated to reflux under vigorous stirring for 2 d. After cooling to room temperature the mixture was extracted with methylene chloride (3×100 mL). The combined organic layers were washed with water (50 mL), dried (MgSO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (300 g, AcOEt/heptane 1:9). 3-Bromo-5-iodo-phenol (21.2 g, 96%) was obtained as pale brown solid.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux
  3. extractionwas extracted with methylene chloride (3×100 mL)
  4. washThe combined organic layers were washed with water (50 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customto give the crude product which
  8. customwas purified by flash chromatography on silica gel (300 g, AcOEt/heptane 1:9)

출처 및 근거

ORD 기록
ord-c82d30573024422aae1fd2c8d0f47fec
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07504401B2

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