Hydrogen Bromide → 4-Bromo-1-(difluoromethoxy)-2-methylbenzene
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]=1Participants
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
- additionAfter the addition
- temperaturethe mixture was heated at 60° C. for 30 minutes
- extractionThe resulting solution was extracted with EtOAc (3×50 mL)
- washthe combined organic layers washed with H2O (1×20 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-53a4e676e9af458f8933b289d9414ad9
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07517884B2
Reaction notes
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