Methylhydroxylamine → HCID 86744247, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]1[CH:13]=[CH:12][C:11](/[C:14](/[CH3:19])=[CH:15]\[C:16](O)=[O:17])=[CH:10]1.[CH3:20][NH:21][OH:22]>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]1[CH:13]=[CH:12][C:11](/[C:14](/[CH3:19])=[CH:15]\[C:16]([N:21]([OH:22])[CH3:20])=[O:17])=[CH:10]1Participants
3
Procedure
Condensation of (Z)-3-[1-(2,6-dimethylphenyl)-1H-pyrrol-3-yl]-2-butenoic acid is condensed with N-methylhydroxylamine as described in example 1(a) to yield (Z)-3-[1-(2,6-dimethylphenyl)-1H-pyrrol-3-yl]-N-hydroxy-N-methyl-2-butenamide, m.p. 158°-160°.
Sources & evidence
- ORD record
- ord-da941d8db0494ee19935ca86646f986a
- Source dataset
- uspto-grants-1990_10
- Patent number
- US04960787
Reaction notes
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