HuagongsheHuagongshe Chemistry Print Report · For research reference only
{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile → HCID 131712624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | {3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile | HCID 53724731 | — |
| Reactant | HCID 131712625 | HCID 131712625 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131712624 | HCID 131712624 | — |
Reaction Steps
25 g of intermediate (A) and 25 g of vinyloxazolidone were dissolved in 150 ml of ethanol and added with 2.5 g of AZBN. The mixture was heated to reflux for 24 hours in a flask provided with stirrer and reflux condenser. At the end, it was cooled, precipitated in ether, washed and dried. The yield was 14.5 g of a product soluble in water and dimethylformamide, containing about 45% w/w of aminoallylidenmalononitrile moieties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307183 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-36eb5025a6974206802640509133f48f |
| Source note | uspto-grants-1981_12 |