Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | {3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile | HCID 53724731 | — |
| Reactant | HCID 76223853 | HCID 76223853 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86738169 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04307183 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-9f92470d065843769ea69b5cf97c08e2 |
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| Source note | uspto-grants-1981_12 |
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