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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231211Generated: November 2, 2026

Phenylhydrazine → HCID 13712337, compound

https://huagongshe.com/reaction/2231211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
Reactant(1-Oxo-3,4-dihydronaphthalen-2(1H)-ylidene)acetic acidHCID 54488542—
SolventEthanolHCID 702—
ProductHCID 13712337HCID 1371233720.6%

Reaction Steps

A mixture of 5 g of 1,2,3,4-tetrahydro-1-oxo-2-naphthylideneacetic acid and 3 g of phenylhydrazine in 100 ml of ethanol is refluxed for 10 hours. The precipitated crystals are collected by filtration, washed with ethanol and dissolved in 50 ml of acetic acid. The solution is refluxed under heating for 8 hours and the acetic acid is distilled off. The residue is extracted with ethyl acetate and the extract is washed with an aqueous sodium hydrogencarbonate solution. After drying over magnesium sulfate anhydride, the solvent is distilled off and to the residue is added ethanol. The precipitated crystals are collected by filtration and recrystallized from ethanol to give 1.4 g of 2-phenyl-5,6-dihydrobenzo[h]cinnolin-3(2H)-one as pale yellow needles, melting at 155°-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782057
Source datasetuspto-grants-1988_11
ORD IDord-854ed0dadd6548e791fd55a2adace05d
Source noteuspto-grants-1988_11