HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 21286379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | HCID 21286380 | HCID 21286380 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21286379 | HCID 21286379 | — |
Reaction Steps
A solution of 7-nitro-1,2,3,4-tetrahydro-1-oxo-2-naphthaleneacetic acid and phenylhydrazine in ethanol is refluxed under heating for 10 hours. The ethanol is distilled off and to the residue is added acetic acid and then the resulting mixture is refluxed under heating for 8 hours. After the acetic acid is distilled off, the mixture is extracted with chloroform and the extract is washed with water. After drying over magnesium sulfate anhydride, the chloroform is distilled off to give 9-nitro-2-phenyl-4,4a,5,6-tetrahydrobenzo[h]cinnolin-3(2H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04782057 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-781c449de9ae4e97ad5b1fb0373e7269 |
| Source note | uspto-grants-1988_11 |