Reaction equation
[Br:1]Br.[CH3:3][C:4]([C:6]1[C:11]([F:12])=[CH:10][CH:9]=[CH:8][C:7]=1[F:13])=[O:5].[CH3:14][S:15][CH3:16]>ClCCl.C(OCC)C>[Br-:1].[CH3:14][S+:15]([CH3:16])[CH2:3][C:4]([C:6]1[C:7]([F:13])=[CH:8][CH:9]=[CH:10][C:11]=1[F:12])=[O:5]Participants
Procedure
A solution of bromine (4.1 ml, 80 mmoles) in dichloromethane (6 ml) was added dropwise to a solution of 2,6-difluoroacetophenone (12.4 g, 80 mmoles) in anhydrous diethyl ether (100 ml). The reaction solution was evaporated and the resulting liquid was dissolved in tetrahydrofuran (150 ml) and methyl sulfide (9 ml, 120 mmoles) was added. The mixture was allowed to stand at room temperature for 6 days (approximately 144 hours). The crystals were filtered to yield 8.9 g (38%) of dimethyl-2,6-difluorophenacylsulfonium bromide. A mixture of the sulfonium salt (8.9 g) and isopropyl nitrate (6.4 ml, 60 mmoles) was stirred in dichloromethane (80 ml) for 7 days (approximately 168 hours) at room temperature. The volatiles were evaporated and the residue was dissolved in diethyl ether (250 ml). The organic solution was washed 4 times with 100 ml portions of water, saturated sodium chloride, dried (sodium sulfate), and evaporated to give 6.8 g of a solid. Recrystallization from carbon tetrachloride (250 ml) gave 4.9 g (23%) of crystals, melting point 138°-140° C.
Workup
- customThe reaction solution was evaporated
- dissolutionthe resulting liquid was dissolved in tetrahydrofuran (150 ml)
- custom(approximately 144 hours)
- filtrationThe crystals were filtered
Sources & evidence
- ORD record
- ord-2aaa0e8df56e4065ba11a7362bf3e362
- Source dataset
- uspto-grants-1985_10
- Patent number
- US04544753
Linked notes
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