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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304425Generated: November 1, 2026

2-Aminobiphenyl → HCID 178509175, compound

https://huagongshe.com/reaction/2304425

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobiphenylHCID 7015—
ReactantMalononitrileHCID 8010—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 21955033HCID 21955033—
ProductHCID 178509175HCID 17850917561%

Reaction Steps

This compound was prepared using 123 mg (0.5 mmol) of 2-[(biphenyl-2-yl)hydrazono]-malononitrile, which was derived from 2-aminobiphenyl (169 mg, 1.0 mmol) and malononitrile (1.5 mmol) as described in Example 8, and hydrazine hydrate. Precipitate formed in the reaction tube immediately after the addition of the hydrazine hydrate then the solution cleared. Very little solid remained 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 85 mg (61%) of the title compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436915B1
Source datasetuspto-grants-2002_08
ORD IDord-a1d8b578c6e14adeae11975db4f8c8aa
Source noteuspto-grants-2002_08