Potassium Carbonate → 4-Bromo-1-(difluoromethoxy)-2-fluorobenzene
Reaction equation
Cl[C:2]([F:7])([F:6])C([O-])=O.[Na+].C(=O)([O-])[O-].[K+].[K+].[Br:15][C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([F:23])[CH:17]=1.[OH-].[Na+]>CCOCC.O.CN(C=O)C>[Br:15][C:16]1[CH:21]=[CH:20][C:19]([O:22][CH:2]([F:7])[F:6])=[C:18]([F:23])[CH:17]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 100 °C
Procedure
To a 100 mL flask charged with DMF (23 mL) was added sodium 2-chloro-2,2-difluoroacetate (4.79 g, 31.4 mmol), potassium carbonate (2.60 g, 18.85 mmol), 4-bromo-2-fluorophenol (3 g, 15.71 mmol). Water (5.75 mL) was added and the reaction mixture was heated to 100° C. for 3 hours. Upon cooling to room temperature, the reaction mixture was diluted with Et2O (100 mL) and a 2 N NaOH solution (100 mL). The organic layer was removed and dried over anhydrous Na2SO4. Upon filtration the organic solution was concentrated on a rotary evaporator with the water bath at 4° C. to yield the title compound as a clear oil (1 g). NMR (400 MHz, CDCl3) δ 7.35 (dd, J=9.7, 2.3 Hz, 1H), 7.27 (ddd, J=8.7, 2.3, 1.5 Hz, 1H), 7.19-7.04 (m, 1H), 6.53 (t, J=73.0 Hz, 1H); ESIMS m/z 242 ([M+H]+).
Workup
- temperatureUpon cooling to room temperature
- customThe organic layer was removed
- dry with materialdried over anhydrous Na2SO4
- filtrationUpon filtration the organic solution
- concentrationwas concentrated on a rotary evaporator with the water bath at 4° C.
Sources & evidence
- ORD record
- ord-58a4e164d7534bc9bdd0563fbd885ce9
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09113629B2
Reaction notes
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