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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304439Generated: October 30, 2026

Malononitrile → HCID 178493283, compound

https://huagongshe.com/reaction/2304439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-(Trifluoromethyl)-m-anisidineHCID 605671—
ReactantHCID 21954979HCID 21954979—
ProductHCID 178493283HCID 1784932837%

Reaction Steps

This compound was prepared using 134 mg (0.5 mmol) of 2-[(3-methoxy-5-trifluoromethylphenyl)hydrazono]malononitrile, which was derived from 3-methoxy-5-trifluoromethylaniline (191 mg, 1.0 mmol) and malononitrile (1.5 mmol) as described in Example 8, and hydrazine hydrate. Very little solid had formed after heating the reaction 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 room 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 10 mg (7%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436915B1
Source datasetuspto-grants-2002_08
ORD IDord-c34cf1fb5fcc4a0098f31f6faa6f3e69
Source noteuspto-grants-2002_08