1-(1,3-Thiazol-5-yl)ethan-1-one → 2-Bromo-1-(thiazol-5-yl)ethanone hydrobromide
Reaction equation
[C:1]([C:4]1[S:8][CH:7]=[N:6][CH:5]=1)(=[O:3])[CH3:2].[BrH:9].[Br:10]CC(C1C=C(C)C=CN=1)=O>>[BrH:10].[Br:9][CH2:2][C:1]([C:4]1[S:8][CH:7]=[N:6][CH:5]=1)=[O:3]Participants
3
Procedure
* 5-bromoacetylthiazole hydrobromide was prepared from 5-acetylthiazole according to the procedure for preparing 2-bromoacetyl-4-methylpyridine hydrobromide described in step 2 of Example 31.
Sources & evidence
- ORD record
- ord-64edddb875d942759324e44cf49c99b8
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
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