1-(3-Methylpyridin-2-yl)ethan-1-one → 2-Bromoacetyl-3-methylpyridine hydrobromide
Reaction equation
[C:1]([C:4]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][N:5]=1)(=[O:3])[CH3:2].[BrH:11].[Br:12]CC(C1C=C(C)C=CN=1)=O>>[BrH:12].[Br:11][CH2:2][C:1]([C:4]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][N:5]=1)=[O:3]Participants
3
Procedure
* 2-Bromoacetyl-3-methylpyridine hydrobromide was prepared from 2-acetyl-3-methylpyridine (T. A. Crabb et al., Org. Magn. Reson., 1982, 20, 242) according to the procedure for preparing 2-bromoacetyl-4-methylpyridine hydrobromide described in step 2 of Example 31.
Sources & evidence
- ORD record
- ord-65a6bf89365d4b18af5a8565a69ee50e
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
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