4-(Chloromethyl)pyridinium chloride → N-Methylpyridine-4-methylamine
Reaction equation
Cl.Cl[CH2:3][C:4]1[CH:9]=[CH:8][N:7]=[CH:6][CH:5]=1.[CH3:10][NH2:11].CCO>>[CH3:10][NH:11][CH2:3][C:4]1[CH:9]=[CH:8][N:7]=[CH:6][CH:5]=1Participants
3
Procedure
Using 4-chloromethyl-pyridine hydrochloride salt and 33% methylamine/EtOH the title compound was obtained as a colourless liquid (0.1 mm Hg, 60-62° C.) (79% yield), MS: m/e=122.1 (M+).
Sources & evidence
- ORD record
- ord-21d110bc722d42a0882ff15ebe6cb6cf
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06963000B2
Reaction notes
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