HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905694Generated: October 30, 2026
(4-Chlorophenyl)hydrazine → HCID 178435590, compound
https://huagongshe.com/reaction/1905694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | HCID 14153005 | HCID 14153005 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 178435590 | HCID 178435590 | — |
Reaction Steps
A solution of 2.6 g of ethyl 4-chloro-6-ethyl-5,6,7,8-tetrahydroquinoline-3-carboxylate in 30 ml n-butanol is treated with 1.38 g of 4-chlorophenylhydrazine at room temperature under nitrogen. After stirring at room temperature overnight, the reaction mixture is heated at reflux for 41/2 hours. The reaction mixture is cooled to room temperature, the precipitate is filtered off, washed with hexane and air-dried to yield a yellow solid. The crude product is dissolved in 30 ml 1N NaOH and extracted with ether. The aqueous layer is then treated with 1.6 g of NH4Cl. The precipitate which forms is filtered off, washed with water, and dried in a vacuum oven at 120° overnight to yield 2,3,6,7,8,9-hexahydro-2-p-chlorophenyl-8-ethylpyrazolo[4,3-c]quinolin-3-(5H)-one, m.p. 318°-320°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04647566 |
|---|
| Source dataset | uspto-grants-1987_03 |
|---|
| ORD ID | ord-ca6856f3db8145ddae2a68581513bb70 |
|---|
| Source note | uspto-grants-1987_03 |
|---|