HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylcyclopropenone → HCID 21462217, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylcyclopropenone | HCID 65057 | — |
| Reactant | Pyridine-3,4-dicarbonitrile | HCID 74211 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 21462217 | HCID 21462217 | — |
Reaction Steps
Diphenylcyclopropenone (0.319 g, 1.55 mmol) and 3,4-dicyanopyridine (0.200 g, 1.55 mmol) were mixed in a dry, argon filled reaction flask. Chlorobenzene (2.5 mL) (oxygen free) was added, and the reaction was heated to 130C. After 2 h the heating was stopped and the reaction was allowed to reach room temperature. Petroleum ether 40-60C (2.5 mL) was added in order to obtain a complete precipitate of the product. The solvent was filtered off and the precipitate was washed with petroleum ether. The crude product was stirred with chloroform (30. mL) for lb. The dark chloroform solution was filtered off leaving the title product as a yellow precipitate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05435991 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-2bd5c21322c742cfb57ecb786c08207f |
| Source note | uspto-grants-1995_07 |