HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → HCID 54566724, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Cyclohexene-1-acetonitrile | HCID 81461 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54566724 | HCID 54566724 | — |
Reaction Steps
In a 50 ml 3-necked round bottom flask equipped with a nitrogen inlet, condensor and magnetic stir bar is placed cinnamaldehyde (2.64 g, 0.02 mol), 1-cyclohexenylacetonitrile (2.42 g, 0.02 mol) and sodium hydroxide (0.2 g, 0.005 mol) in absolute ethanol (25 ml). The reaction is stirred at room temperature until completion, during which time the crude product precipitates from solution. The precipitate is filtered, washed with water and dried. Recrystallization from ethanol yields a yellowish solid with maximum absorption at 338 nm and extinction coefficient of 45,825.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935533 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-46eec831cee04862a60a82141c1d74ac |
| Source note | uspto-grants-1990_06 |