1-(1-Methyl-1H-imidazol-2-yl)ethan-1-one → 2-Bromoacetyl-1-methylimidazole hydrobromide
Reaction equation
[C:1]([C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][N:8]=1)(=[O:3])[CH3:2].[BrH:10].[Br:11]CC(C1C=C(C)C=CN=1)=O>>[BrH:11].[Br:10][CH2:2][C:1]([C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][N:8]=1)=[O:3]Participants
3
Procedure
* 2-bromoacetyl-1-methylimidazole hydrobromide was prepared from 2-acetyl-1-methylimidazole according to the procedure for preparing 2-bromoacetyl-4-methylpyridine hydrobromide described in step 2 of Example 31.
Sources & evidence
- ORD record
- ord-608ea322a2494c648f1f99f11e9ed403
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
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