HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetaldehyde → 1-Cyano-1-(4-diethylaminophenyl)cyclopentane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | Ethanol | HCID 702 | — |
| Edukt | 1-(4-Nitrophenyl)cyclopentane-1-carbonitrile | HCID 4351905 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Produkt | 1-Cyano-1-(4-diethylaminophenyl)cyclopentane | HCID 19834117 | — |
Reaktionsschritte
In a pressure reactor was placed 43.4 g (0.2 mole) of 1-cyano-1-(4-nitrophenyl)cyclopentane and 500 mL of absolute ethanol. One gram of 5% Pd/C was added, the reactor charged with hydrogen and shaken at room temperature until the theoretical amount of hydrogen had been taken up. The reactor was vented and 22 g (0.5 mole) of acetaldehyde and 2 g of 10% Pd/C was added. The reactor was charged with hydrogen and shaken at room temperature for 16 hours. The reaction mixture was then filtered and the filtrate concentrated in vacuo. The product was purified by chromatography, using a gradient of 90% hexane: 10% ethylacetate to 70% hexane: 30% ethylacetate as eluant. There was obtained 10.7 g of a clear oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05015644 |
| Quelldatensatz | uspto-grants-1991_05 |
| ORD ID | ord-0ad487086dea4a00aeb59f61f85a9439 |
| Quellennotiz | uspto-grants-1991_05 |