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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660303Generated: November 3, 2026

Acrylamide → HCID 86738169, compound

https://huagongshe.com/reaction/1660303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
Reactant{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrileHCID 53724731—
ReactantHCID 76223853HCID 76223853—
SolventEthanolHCID 702—
ProductHCID 86738169HCID 86738169—

Reaction Steps

A solution of 120 g of acrylamide and 114 g of 3-diallylaminoallylidenmalononitrile (A) in 500 ml of ethanol was brought to reflux. 3.2 g of 2,2'-azobisisobutyrronitrile (AZBN) were added thereto and the mixture was left to reflux for 1 hour under stirring. A solution of 104 g of acrylamide, 800 ml of ethanol and 3.2 g of AZBN was then introduced therein. The obtained solution was left to reflux for 1 hour under stirring. A solution of 88 g of acrylamide, 400 ml of ethanol and 2.4 g of AZBN was introduced therein and the solution was left to reflux for 1 hour. A solution of 72 g of acrylamide, 400 ml of ethanol and 1.6 g of AZBN was added thereto and the obtained solution was left to reflux for 1 hour. A solution of 56 g of acrylamide, 400 ml of ethanol and 1.6 g of AZBN was finally added thereto and the obtained solution was left to reflux for 2 hours. The so-obtained mixture was cooled, filtered, washed with ethanol and then with ethyl ether and dried under vacuum at 50° C., thus obtaining 478 g of a water soluble product containing about 9% w/w of aminoallylidenmalononitrile moieties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307183
Source datasetuspto-grants-1981_12
ORD IDord-9f92470d065843769ea69b5cf97c08e2
Source noteuspto-grants-1981_12