o-(Trifluoromethyl)benzaldehyde → Pyridine, 2-methyl-6-[2-(trifluoromethyl)phenyl]-
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.[F:15][C:16]([F:26])([F:25])C1C=CC=CC=1C=O>>[F:15][C:16]([F:26])([F:25])[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-trifluoromethylphenyl)-2-methylpyridine was prepared substantially according to the procedures of Example 1 for prearing 6-(2-chlorophenyl)-2-methylpyridine except 2-trifluoromethylbenzaldehyde was used to afford 6-(2-trifluoromethylphenyl)-2-methylpyridine.
Workup
- custom6-(2-trifluoromethylphenyl)-2-methylpyridine was prepared substantially
Sources & evidence
- ORD record
- ord-03bd82f2f90a480aa393eab757c7bf08
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04696938
Reaction notes
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