Diethyl Ether → 7-Bromo-1-benzofuran

HRID 2266226Notes

Reaction equation

HRID 2266226 reaction equation
C(O[CH:4](OCC)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[Br:13])C.[OH-].[Na+].CCOCC>ClC1C=CC=CC=1>[Br:13][C:8]1[C:7]2[O:6][CH:5]=[CH:4][C:12]=2[CH:11]=[CH:10][CH:9]=1

Participants

5

Procedure

A stirred mixture of polyphosphoric acid (˜5 g) and chlorobenzene (8 mL) was heated at reflux and a solution of 1-(2,2-diethoxyethoxy)-2-bromobenzene (2.62 g, 9.0 mmol) in chlorobenzene (3 mL) was added dropwise over 10 min. The mixture was heated at reflux for 1.5 h. The mixture was allowed to cool to rt and 1M aq NaOH (20 mL) was added, followed by ether (175 mL). The mixture was washed with water (2×20 mL) and brine (20 mL), and dried over MgSO4. Evaporation of the solvent left a residue which was purified by a chromatography on a 140-g silica cartridge eluted with hexanes and a 0-10% EtOAc in hexanes gradient. Appropriate fractions were pooled and concentrated to afford 7-bromobenzofuran (0.65 g, 38% from 2-bromophenol) as a clear colorless oil.

Workup

  1. temperaturewas heated
  2. temperatureat reflux
  3. temperatureThe mixture was heated
  4. temperatureat reflux for 1.5 h
  5. washThe mixture was washed with water (2×20 mL) and brine (20 mL)
  6. dry with materialdried over MgSO4
  7. customEvaporation of the solvent
  8. waitleft a residue which
  9. customwas purified by a chromatography on a 140-g silica cartridge
  10. washeluted with hexanes
  11. concentrationconcentrated

Sources & evidence

ORD record
ord-388a6841169e4b118d7ebf45649d8d69
Source dataset
uspto-grants-2010_12
Patent number
US07858624B2

Reaction notes

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