HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cinnamoylbenzene → 3,4,6-Triphenyloxan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cinnamoylbenzene | HCID 7189 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,4,6-Triphenyloxan-2-one | HCID 20395893 | — |
Reaction Steps
20.8 g (0.1 mol) of chalcone (1,3-diphenyl 1-propenone) are dissolved hot in 12.0 g (0.102 mol) of benzyl cyanide. 60 ml of hexane-absolute alcohol mixture (20-80) are added; the reaction medium is cooled to 0° C. in an ice-salt mixture. The catalyst (8 ml of 2 N ethanol KOH) is then added slowly. Crystallisation intervenes very quickly in the vessel, about 1 hour after the beginning of pouring which lasts 3/4 of an hour. The vessel is then placed in the refrigerator for the night.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163799 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-8ec93865fefd40039cdb1980af72a991 |
| Source note | uspto-grants-1979_08 |