HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3,4-Dihydro-2H-4-chromenylidene)acetonitrile → 2-(Chroman-4-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3,4-Dihydro-2H-4-chromenylidene)acetonitrile | HCID 56984834 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Chroman-4-yl)acetonitrile | HCID 13362781 | — |
Reaction Steps
The unsaturated compound obtained in Step A (Z+E mixture), solubilised in ethanol (20 ml), is introduced into the reactor of a Parr apparatus. 10% (by weight) palladium-on-carbon is then added. The double bond is hydrogenated at a pressure of 45 psi for 12 hours. The catalyst is removed by filtration; the solvent is then evaporated. The residual oil is purified on a silica column eluted by a mixture of AcOEt/PE 3/7. Colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06602903B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-5e8b3bae9636410ab4676fbaad6cae90 |
| Source note | uspto-grants-2003_08 |