HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Chlorophenyl)hydrazine → HCID 178423471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | HCID 13713231 | HCID 13713231 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178423471 | HCID 178423471 | — |
Reaction Steps
A mixture of 1.37 g of p-chlorophenylhydrazine and 2.4 g of ethyl 4-chloro-6-methyl-5,6,7,8-tetrahydroquinoline-3-carboxylate in 75 mL of xylene is stirred and refluxed overnight, then cooled to room temperature and filtered. Collected solid is dissolved in hot ethanol, treated with decolorizing charcoal, and concentrated to a smaller volume to deposit a solid, which is recrystallized from ethanol containing hydrogen chloride to yield 2-p-chlorophenyl-2,3,6,7,8,9-hexahydro-8-methylpyrazolo[4,3-c]quinolin-3(5H)-one hydrochloride, m.p. 331°-333°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04602014 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-0b219f1bde2b4c76ba3d5ecfd0e09fbf |
| Source note | uspto-grants-1986_07 |