1-Bromo-3-fluorobenzene → HCID 14032496, compound
Reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[F:5][C:6]1[CH:7]=[C:8]([Br:12])[CH:9]=[CH:10][CH:11]=1.[C:13]([N:16]1[CH2:24][CH2:23][CH:19]([C:20](Cl)=[O:21])[CH2:18][CH2:17]1)(=[O:15])[CH3:14]>>[Br:12][C:8]1[CH:9]=[CH:10][C:11]([C:20]([CH:19]2[CH2:18][CH2:17][N:16]([C:13](=[O:15])[CH3:14])[CH2:24][CH2:23]2)=[O:21])=[C:6]([F:5])[CH:7]=1Participants
4
Procedure
To a stirred suspension of 21.1 g of aluminum chloride and 63 ml of 3-fluorobromobenzene was added, portionwise, 16.0 g of 1-acetylisonipecotoyl chloride. The reaction mixture was stirred under reflux for 4 hrs. Most of the supernatant 3-fluorobromobenzene was decanted and ice water was added. The aqueous mixture was extracted with dichloromethane and the extract was washed with water, dried over anhydrous magnesium sulfate and the solvent concentrated to give an oil. The oil was triturated with ether and a solid separated out. Recrystallization of the solid from cyclohexane gave 4.9 g (19%) of product. Recrystallization from cyclohexane yielded the analytical sample, mp 111°-113° C.
Workup
- additionwas added
- temperatureunder reflux for 4 hrs
- customMost of the supernatant 3-fluorobromobenzene was decanted
- additionice water was added
- extractionThe aqueous mixture was extracted with dichloromethane
- washthe extract was washed with water
- dry with materialdried over anhydrous magnesium sulfate
- concentrationthe solvent concentrated
- customto give an oil
- customThe oil was triturated with ether
- customa solid separated out
- customRecrystallization of the solid from cyclohexane
Sources & evidence
- ORD record
- ord-5bc88e9cdcbe4a5eb844c4ec162cf17f
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04775761
Reaction notes
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