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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254952Generated: October 30, 2026

Malononitrile → HCID 178509183, compound

https://huagongshe.com/reaction/254952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant[4-(Trifluoromethyl)phenyl]carbonohydrazonoyl dicyanideHCID 2781638—
ProductHCID 178509183HCID 178509183—

Reaction Conditions

Temperature75 °C

Reaction Steps

4-[(4-trifluoromethylphenyl)hydrazono]-4H-pyrazole-3,5-diamine was prepared using 119 mg (0.5 mmol) of 2-[(4-trifluoromethylphenyl)hydrazono]malononitrile, which was derived from 4-(trifluoromethyl)aniline (126 μL, 1.0 mmol) and malononitrile (1.5 mmol), and hydrazine hydrate. No precipitate had formed after heating at 75° C. for 1 hr, 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 ethyl acetate and then precipitated by the addition of hexanes. The resulting solid was isolated by filtration and dried to yield 67 mg (50%) of the compound as a greenish brown solid; 1H NMR (ppm, DMSO-d6): 6.03 (br s, 2H), 6.48 (br s, 2H), 7.63 (d, 2H), 7.80 (d, 2H), 10.80 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875728B2
Source datasetuspto-grants-2011_01
ORD IDord-ebcc09c3b535471bb8e3edd3fb2b7b17
Source noteuspto-grants-2011_01