Pyridine → 1-(2-Oxo-2-phenylethyl)pyridin-1-ium bromide
Reaction equation
[CH2:1]([Br:10])[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3].[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[Br-:10].[CH2:1]([N+:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3]Participants
3
Procedure
N-phenacylpyridinium bromide was prepared by slowly adding phenacyl bromide to a stirred flask containing an equimolar quantity of pyridine. The slightly exothermic reaction was accompanied by the precipitation of the solid N-phenacylpyridinium bromide. The salt was then filtered and washed thoroughly with anhydrous ether.
Workup
- customThe slightly exothermic reaction
- customwas accompanied by the precipitation of the solid N-phenacylpyridinium bromide
- filtrationThe salt was then filtered
- washwashed thoroughly with anhydrous ether
Sources & evidence
- ORD record
- ord-3d92c6ce28bb4247ba978dfcc6f0040c
- Source dataset
- uspto-grants-1979_11
- Patent number
- US04175973
Reaction notes
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