O-ethylhydroxylamine hydrochloride → HCID 54360874, compound
Reaction equation
[CH2:1]([CH:4]([CH2:14][O:15][CH2:16][CH2:17][CH2:18][NH:19][CH:20]([CH3:22])[CH3:21])[CH2:5][C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=O)[CH:2]=[CH2:3].Cl.[CH2:24]([O:26][NH2:27])[CH3:25]>>[CH2:24]([O:26][N:27]=[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH2:5][CH:4]([CH2:1][CH:2]=[CH2:3])[CH2:14][O:15][CH2:16][CH2:17][CH2:18][NH:19][CH:20]([CH3:22])[CH3:21])[CH3:25]Participants
3
Procedure
The procedure described in Example 88 was repeated using 3-allyl-4-(3-[N-isopropylamino]propoxy)butyrophenone and ethoxyamine hydrochloride to give 3-allyl-4-(3-[N-isopropylamino)propoxy)-butyrophenone O-ethyloxime as a solid, m.p. 124°-126° C.
Sources & evidence
- ORD record
- ord-c132c3593d2d4aadb511610c6cf83f98
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05866611
Reaction notes
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