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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660305Generated: November 3, 2026

{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile → HCID 131712624, compound

https://huagongshe.com/reaction/1660305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrileHCID 53724731—
ReactantHCID 131712625HCID 131712625—
SolventEthanolHCID 702—
ProductHCID 131712624HCID 131712624—

Reaction Steps

25 g of intermediate (A) and 25 g of vinyloxazolidone were dissolved in 150 ml of ethanol and added with 2.5 g of AZBN. The mixture was heated to reflux for 24 hours in a flask provided with stirrer and reflux condenser. At the end, it was cooled, precipitated in ether, washed and dried. The yield was 14.5 g of a product soluble in water and dimethylformamide, containing about 45% w/w of aminoallylidenmalononitrile moieties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307183
Source datasetuspto-grants-1981_12
ORD IDord-36eb5025a6974206802640509133f48f
Source noteuspto-grants-1981_12