HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Allyl-4-hydroxybenzonitrile → 4-hydroxy-3-propylBenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Allyl-4-hydroxybenzonitrile | HCID 258442 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-hydroxy-3-propylBenzonitrile | HCID 13987669 | 99.6% |
Reaction Steps
A Parr hydrogenation shaker was charged with a solution of 29.76 g (187 mmol) of the product of Step A in 100 mL of ethanol and 3.00 g of a 10% palladium on carbon catalyst was added. The flask was mounted in the hydrogenation appartus, freed of air, pressurized with hydrogen (40 psig) and shaken 80 minutes. At the end of this preiod, TLC analysis (15% ethyl acetate/hexane) indicated that the reaction was complete and the reaction mixture was filtered and evaporated. The product was dried in vacuo to afford 30.01 g (99%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05565485 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-ac7037940627436d94a0c8b14635c28f |
| Source note | uspto-grants-1996_10 |