Hydrogen Bromide → 4-Bromo-1-(difluoromethoxy)-2-methylbenzene

HRID 2110138Notes

Reaction equation

HRID 2110138 reaction equation
N[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:9]([F:11])[F:10])=[C:4]([CH3:12])[CH:3]=1.N([O-])=O.[Na+].[BrH:17]>O.[Cu]Br>[Br:17][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:9]([F:11])[F:10])=[C:4]([CH3:12])[CH:3]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 4-amino-1-difluoromethoxy-2-methyl-benzene (5 g, 28.90 mmol) in HBr (20 mL) and water (20 mL) at 0° C. was added a solution of sodium nitrite (2.07 g, 30.00 mmol) in H2O (10 ml) dropwise over a period of 20 minutes. After the addition was complete, the reaction mixture was stirred for 30 minutes at 0° C. Copper (I) bromide (4 g, 27.87 mmol) was then added and the mixture was heated at 60° C. for 30 minutes. The resulting solution was extracted with EtOAc (3×50 mL) and the combined organic layers washed with H2O (1×20 mL), dried over Na2SO4 and concentrated to provide 2.5 g (37%) of 4-bromo-1-(difluoromethoxy)-2-methylbenzene.

Workup

  1. additionAfter the addition
  2. temperaturethe mixture was heated at 60° C. for 30 minutes
  3. extractionThe resulting solution was extracted with EtOAc (3×50 mL)
  4. washthe combined organic layers washed with H2O (1×20 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-53a4e676e9af458f8933b289d9414ad9
Source dataset
uspto-grants-2009_04
Patent number
US07517884B2

Reaction notes

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