HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 21286394, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | HCID 21286384 | HCID 21286384 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21286394 | HCID 21286394 | — |
Reaction Steps
After a mixture of 7-trifluoromethyl-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. To the residue is added acetic acid and the mixture is refluxed under heating for 7 hours. After the acetic acid is distilled off, the residue is extracted with chloroform and the extract is washed with water and dried over magnesium sulfate anhydride. The chloroform is distilled off to give 2-phenyl-9-trifluoromethyl-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-1b6887008fd142e1a95e52c971b70d2b |
| Source note | uspto-grants-1988_11 |