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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660302Generated: November 1, 2026

Acrylic Acid → HCID 86738178, compound

https://huagongshe.com/reaction/1660302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
ReactantLauroyl peroxideHCID 7773—
Reactant{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrileHCID 53724731—
SolventEthanolHCID 702—
ProductHCID 86738178HCID 86738178—

Reaction Steps

60 g. of intermediate (A) and 20 g. of acrylic acid were diluted in 120 cc. of ethanol in a flask with stirrer and reflux and 2 g. of lauroyl peroxide were added, and then reflux heated. After one hour, 16 g. of acrylic acid and 1 g. of lauroyl peroxide diluted in 20 g. of ethanol were added; always continuing the reflux heating, at one hour time intervals the following additions were made: 13 g. of acrylic acid and 1 g. of lauroyl peroxide in 20 cc. of ethanol; 10 g. of acrylic acid and 0.8 g. of lauroyl peroxide in 15 cc. of ethanol; 8 g. of acrylic acid and 0.8 g. of lauroyl peroxide in 10 cc. of ethanol. After the last addition the mixture was refluxed for two hours, then it was cooled, and precipitated in ethyl ether; the precipitate was recovered on filter, washed with ether and vacuum dried at 50° C. The yield was 49 g. of a product containing about 23% of aminoallylidenemalononitrile units. The product was water and NaOH at pH=7 soluble. A solution at 6% 1:9000 diluted with water, had an optical density of 0.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307184
Source datasetuspto-grants-1981_12
ORD IDord-a0b8294ef8bb4614a6514ded73313b26
Source noteuspto-grants-1981_12