Bromine → 4-Bromo-2-fluoroanisole

HRID 653815Notes

Reaction equation

HRID 653815 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].[Br:10]Br>C(Cl)(Cl)Cl>[F:1][C:2]1[CH:7]=[C:6]([Br:10])[CH:5]=[CH:4][C:3]=1[O:8][CH3:9]

Participants

4

Procedure

306 g of 2-fluoroanisole was dissolved in 750 ml of chloroform. To the resulting solution, was added dropwise 389 g of bromine under stirring at room temperature. After the completion of the addition, the reaction mixture was heated under reflux for nine hours and then allowed to cool to room temperature. The mixture was washed with 500 ml of a 5% aqueous solution of sodium hydroxide and then the organic layer was washed with 500 ml portions of water thrice. The organic layer was separated and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by distillation (main fraction: 14 mmHg, 98°-100° C.) to thereby give 454 g of 2-fluoro-4-bromoanisole. Yield: 91%.

Workup

  1. additionAfter the completion of the addition
  2. temperaturethe reaction mixture was heated
  3. temperatureunder reflux for nine hours
  4. temperatureto cool to room temperature
  5. washThe mixture was washed with 500 ml of a 5% aqueous solution of sodium hydroxide
  6. washthe organic layer was washed with 500 ml portions of water thrice
  7. customThe organic layer was separated
  8. dry with materialdried over anhydrous sodium sulfate
  9. distillationAfter distilling off the solvent
  10. distillationthe residue was purified by distillation (main fraction: 14 mmHg, 98°-100° C.)

Sources & evidence

ORD record
ord-9e10d4a663954720b2b39200c1d3e11c
Source dataset
uspto-grants-1992_07
Patent number
US05128472

Reaction notes

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