2-Bromobenzaldehyde → 6-(2-Bromophenyl)-2-methylpyridine
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]([CH3:14])[CH:11]=[CH:10][CH:9]=1.[Br:15]C1C=CC=CC=1C=O>>[Br:15][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]([CH3:14])[CH:11]=[CH:10][CH:9]=1Participants
3
Procedure
6-(2-bromophenyl)-2-methylpyridine was prepared substantially according to the procedure of Example 1 for preparing 6-(2-chlorophenyl)-2-methylpyridine except 2-bromobenzaldehyde was used to afford 6-(2-bromophenyl)-2-methylpyridine.
Workup
- custom6-(2-bromophenyl)-2-methylpyridine was prepared substantially
Sources & evidence
- ORD record
- ord-fbfa25e8004d49ec864de2aac69874bd
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04696938
Reaction notes
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