Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | {3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile | HCID 53724731 | — |
| Reactant | HCID 76223853 | HCID 76223853 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86738173 | HCID 86738173 | — |
Reaction Steps
40 g of intermediate (A) and 10.6 g of allylamine in 580 ml of ethanol and 19.6 ml of 37% hydrochloric acid were dissolved in a flask provided with a stirrer and reflux condenser. Under stirring and raising the mixture temperature up to 90° C., a solution of 107.7 g of acrylamide and 4.2 g of 2.2'-azobisisobutyrronitrile in 648 ml of ethanol was added thereto. The reaction mixture was kept at 90° C. for 20 hours and then poured into 2 liters of acetone; the precipitated product was grinded and washed upon decantation with one liter of acetone, filtered and dried. 108.6 g of a water soluble product were obtained, containing about 10% 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-a60e6d99b61b434c860080d62dc466b7 |
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| Source note | uspto-grants-1981_12 |
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