Hydrogen Peroxide → HCID 178513670, compound
Reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[O:7])=[CH:4][N:3]=1.[OH:11]O>C(O)(=O)C>[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[O:7])=[CH:4][N+:3]=1[O-:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
6-Aminonicotinamide, 50 g, was dissolved in warm glacial acetic acid, 500 ml. To this clear solution 30% hydrogen peroxide, 80 ml was slowly added with agitation. The mixture was then heated to 100° C. for 5 hours. The light brownish solution thus formed was evaporated to a syrupy residue which crystallized on cooling in an ice water bath. The crystals were washed with acetone and dried. The yield of practically pure 6-aminonicotinamide-1-oxide was 51.6 g. This product had a mobility (Rf) of 0.48 on thin-layer chromatogram using a solvent system of benzene:methanol, 1:1.
Workup
- customThe light brownish solution thus formed
- customwas evaporated to a syrupy residue which
- customcrystallized
- temperatureon cooling in an ice water bath
- washThe crystals were washed with acetone
- customdried
Sources & evidence
- ORD record
- ord-742f6226183842edbb49167c203bc23b
- Source dataset
- uspto-grants-1979_02
- Patent number
- US04141977
Reaction notes
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