Pyridine → 1-[2-([1,1'-Biphenyl]-4-yl)-2-oxoethyl]pyridin-1-ium bromide
Reaction equation
[C:1]1([C:7]2[CH:16]=[CH:15][C:10]([C:11](=[O:14])[CH2:12][Br:13])=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[Br-:13].[C:1]1([C:7]2[CH:16]=[CH:15][C:10]([C:11](=[O:14])[CH2:12][N+:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
The title compound was prepared similarly to Example 1 from 4-phenylphenacyl bromide and pyridine in a yield of 95%.
Sources & evidence
- ORD record
- ord-6e582fe245ee4a78872d492460735a45
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05541032
Reaction notes
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