Hydrogen Peroxide → HCID 178514232, compound
Reaction equation
[N+:1]([C:4]1[C:8]([C:9]#[N:10])=[CH:7][NH:6][N:5]=1)([O-:3])=[O:2].[OH:11]O.[OH-].[Na+:14]>CO>[Na+:14].[N+:1]([C:4]1[C:8]([C:9]([NH-:10])=[O:11])=[CH:7][NH:6][N:5]=1)([O-:3])=[O:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 45 °C
Procedure
A solution was made of 8 gm. of 1-sodium salt of 3-nitro-4-pyrazolecarbonitrile in methanol, and 75 ml. of 15% H2O2 was added, followed by 5 ml. of 6 N NaOH. The reaction mixture was heated to 45° C., at which point external cooling was needed to maintain the mixture at 45°-50° C. After the exothermic reaction had subsided, the mixture was held at 45°-50° C. and stirred for 4 hours. Then the mixture was cooled and the methanol was evaporated under vacuum. The liquid remaining was cooled in an ice bath and the product was separated by filtration and dried under vacuum. The dry product was determined to be 8 gm. of 3-nitro-4-pyrazolecarboxamide sodium salt, m.p.>300° C.
Workup
- temperatureexternal cooling
- temperatureto maintain the mixture at 45°-50° C
- customAfter the exothermic reaction
- customwas held at 45°-50° C.
- temperatureThen the mixture was cooled
- customthe methanol was evaporated under vacuum
- temperatureThe liquid remaining was cooled in an ice bath
- customthe product was separated by filtration
- customdried under vacuum
Sources & evidence
- ORD record
- ord-c6ea557b78624f638bafc3f036d56894
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04235995
Reaction notes
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