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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905681Generated: November 2, 2026

(4-Chlorophenyl)hydrazine → HCID 178423471, compound

https://huagongshe.com/reaction/1905681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)hydrazineHCID 70624—
ReactantHCID 13713231HCID 13713231—
SolventO-XyleneHCID 7237—
ProductHCID 178423471HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04647566
Source datasetuspto-grants-1987_03
ORD IDord-7ce919abb47847c9b2927fe6893466e2
Source noteuspto-grants-1987_03