Chlorodifluoromethane → 1,3-Dibromo-5-(difluoromethoxy)benzene
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([Br:8])[CH:7]=1.Cl[CH:11]([F:13])[F:12]>CC(O)C.[OH-].[K+].O>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH:11]([F:13])[F:12])[CH:5]=[C:6]([Br:8])[CH:7]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
To a tared, sealed 350 mL round-bottomed pressure flask containing a solution of 3,5-dibromophenol (10.0 g, 39.7 mmol; see Example 27(ii) above) in 2-propanol (100 mL) and 30% KOH (80 mL) at −78° C. was added chlorodifluoromethane via bubbling for 15 min through the septum. The septum was replaced with a Teflon stopper and the flask was then sealed and allowed to warm to room temperature where the flask was weighed and determined to contain 12.0 g (138 mmol) of chlorodifluoromethane. The solution was refluxed overnight in an oil bath set at 80° C. The flask was cooled to room temperature, the pressure cautiously released and the contents diluted with H2O (200 mL). The aqueous layer was extracted with CHCl3 (2×150 mL), then the combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by Kugelrohr distillation at 80° C. at 0.2 mm Hg to afford the sub-title compound (9.6 g, 80%) as clear liquid.
Workup
- customsealed 350 mL round-bottomed pressure flask
- customvia bubbling for 15 min through the septum
- customthe flask was then sealed
- temperatureThe solution was refluxed overnight in an oil bath
- customset at 80° C
- temperatureThe flask was cooled to room temperature
- extractionThe aqueous layer was extracted with CHCl3 (2×150 mL)
- dry with materialthe combined organics were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- distillationThe residue was purified by Kugelrohr distillation at 80° C. at 0.2 mm Hg
Sources & evidence
- ORD record
- ord-6f4782c52bf34aa78a447b08f1c2c679
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07129233B2
Reaction notes
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