Hydroxyamine hydrochloride → 1-Oximino-2-(4-phenylsemicarbazono)-3-indanone
Reaction equation
Cl.[NH2:2][OH:3].C([O-])(=O)C.[Na+].[C:9]1([NH:15][C:16](=[O:30])[NH:17][N:18]=[C:19]2[C:27](=[O:28])[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:20]2=O)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>O.C(O)C>[N:2](=[C:20]1[C:21]2[C:26](=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:27](=[O:28])[C:19]1=[N:18][NH:17][C:16]([NH:15][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:30])[OH:3]Participants
6
Procedure
0.01 mol of hydroxylamine hydrochloride and 0.01 mol sodium acetate in solution in 20 ml water were added to a solution of 0.01 mol of 2-(4-phenyl semicarbazono)-indan-1,3-dione in 150 ml ethanol. The reaction mixture was refluxed for 1 hour, then the ethanol was eliminated at reduced pressure. The resulting crystals were dried on suction pump, washed in water, dried and recrystallised from isopropanol.
Workup
- temperatureThe reaction mixture was refluxed for 1 hour
- customThe resulting crystals were dried on suction pump
- washwashed in water
- customdried
- customrecrystallised from isopropanol
Sources & evidence
- ORD record
- ord-88092d8900e44ae1a04e9fa8f59ae486
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05571843
Reaction notes
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