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Hydrogen Bromide → 3-Bromo-5-iodophenol

HRID 1784829
Notes
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Reaction equation

HRID 1784829 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

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

Product 1

HCID 226301823-Bromo-5-iodophenolYield 352.9%

Reagents, catalysts & solvents 2

HCID 74236Tetrabutylammonium BromideCatalystHCID 176Acetic AcidSolvent

Procedure

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.

Workup

  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)

Sources & evidence

ORD record
ord-c82d30573024422aae1fd2c8d0f47fec
Source dataset
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07504401B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes