Water → HCID 178514932, compound
Reaction equation
N[C:2]1[CH:15]=[CH:14][C:13]2[O:12][C:11]3[C:6](=[CH:7][CH:8]=[C:9]([C:16]4[NH:20][N:19]=[N:18][N:17]=4)[CH:10]=3)[C:5](=[O:21])[C:4]=2[CH:3]=1.N([O-])=[O:23].[Na+].O>S(=O)(=O)(O)O>[OH:23][C:2]1[CH:15]=[CH:14][C:13]2[O:12][C:11]3[C:6](=[CH:7][CH:8]=[C:9]([C:16]4[NH:20][N:19]=[N:18][N:17]=4)[CH:10]=3)[C:5](=[O:21])[C:4]=2[CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 15 °C
Procedure
The aminoxanthone from step (C) (14.4 g) was dissolved in concentrated sulphuric acid (250 ml) and to the stirred solution at 10°-15° C. was added in portions sodium nitrite (3.6 g). The solution was then stirred at 15° C. for 1 hr, poured on to ice (2 kg) and water (2.5 l). The mixture was slowly brought to the broil and boiled under reflux for 1 hr. The resulting yellow product was filtered off, washed well with water and dried.
Workup
- temperatureunder reflux for 1 hr
- filtrationThe resulting yellow product was filtered off
- washwashed well with water
- customdried
Sources & evidence
- ORD record
- ord-9701b9b4064a4d1082b62f7de535a177
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04902701
Reaction notes
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