Sodium Tetrafluoroborate → HCID 22364564, compound
Reaction equation
[Br-].[CH3:2][O:3][C:4]1[CH:18]=[CH:17][C:7]([C:8](=[O:16])[CH2:9][N+:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1.[F:19][B-:20]([F:23])([F:22])[F:21].[Na+]>>[F:19][B-:20]([F:23])([F:22])[F:21].[CH3:2][O:3][C:4]1[CH:5]=[CH:6][C:7]([C:8](=[O:16])[CH2:9][N+:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:17][CH:18]=1Participants
3
Procedure
The title compound was prepared similarly to Example 2 from 4-methoxyphenacylpyridinium bromide and sodium tetrafluoroborate in a yield of 85%.
Sources & evidence
- ORD record
- ord-67fff2bed73549c2b4f815639d88c63e
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05541032
Reaction notes
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