Hydrogen Peroxide → HCID 22758561, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:15])[CH:9]=[CH:10][C:11]([NH:13][CH3:14])=[O:12])=[CH:4][CH:3]=1.OO.C(O)(=[O:21])C=C.CN>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH:9]2[O:21][CH:10]2[C:11]([NH:13][CH3:14])=[O:12])=[O:15])=[CH:6][CH:7]=1Participants
5
Procedure
3 was prepared as a white solid, m.p.: 160°-161° C, from 4-(4-chlorophenyl)-N-methyl-4-oxo-2-butenamide (3A) by hydrogen peroxide oxidation by the procedure described in Example 1, 3A having been prepared from the corresponding acrylic acid and monomethylamine by the procedure described in Example 2.
Sources & evidence
- ORD record
- ord-27247c51ce6c48f48a4f793593051327
- Source dataset
- uspto-grants-1978_05
- Patent number
- US04091221
Reaction notes
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