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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254978Generated: October 26, 2026

Aniline → 1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamine

https://huagongshe.com/reaction/254978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMalononitrileHCID 8010—
Reactant4-Bromophenylhydrazine hydrochlorideHCID 12157—
ReactantSodium HydroxideHCID 14798—
ReactantCarbonyl cyanide phenylhydrazoneHCID 67541—
Product1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamineHCID 135443434—

Reaction Steps

1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamine was prepared using 85 mg (0.5 mmol) of 2-(phenylhydrazono)malononitrile, which was derived from aniline (10 mL, 107 mmol) and malononitrile (161 mmol), and 4-bromophenylhydrazine hydrochloride (112 mg, 0.5 mmol) with the addition of 0.5 mL of 5% sodium hydroxide solution. Solids had not formed after heating the reaction at 75° C. for 3 hrs, however, analysis of the reaction solution by TLC indicated that no starting material remained. The solution was allowed to cool to ambient temperature and the solvent was evaporated. The residue was dissolved in methanol and then precipitated by the addition of water. The resulting solid was isolated by filtration and dried to yield 49 mg (27%) of the compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875728B2
Source datasetuspto-grants-2011_01
ORD IDord-7d05be4dceed4a2f9344bec6b52aace1
Source noteuspto-grants-2011_01