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 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86738175 | HCID 86738175 | — |
Reaction Steps
In a 10 liters flask, supplied with stirrer, reflux and internal thermometer, 230 g. of acrylamide and 120 g. of 3-diallylaminoallylidenemalononitrile (A) were dissolved in 4 liters of ethanol at 96%. The mixture temperature was increased to 78° C. under agitation. 8 g. of 2,2'-azobisisobutyrronitrile (AZBN) were introducted at this point. After 10 minutes, a yellowish product began separating. The reaction was continued under those conditions for 14 hours. The mixture was then cooled at room temperature; the separated product was filtered, washed with diethyl ether and vacuum dried at 50° C. The yield of the solid yellowish product was 320 g., with 8% aminoallylidenemalononitrile units in weight. The IR, spectrophotometric analysis and the TLC confirmed for the polymer a structure with allylidenemalononitrile groups. The solution at 6% in 70/30 water/ethanol diluted 1:2000 in water showed an optical density of 0.7 at 382 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04307184 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-9047c868830240c1aa6f84b0a0cf26cb |
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| Source note | uspto-grants-1981_12 |
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