化工社化工社 化学情報印刷レポート · 研究参考用
Acetaldehyde → 1-Cyano-1-(4-diethylaminophenyl)cyclopentane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 1-(4-Nitrophenyl)cyclopentane-1-carbonitrile | HCID 4351905 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 生成物 | 1-Cyano-1-(4-diethylaminophenyl)cyclopentane | HCID 19834117 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05015644 |
| 出典データセット | uspto-grants-1991_05 |
| ORD ID | ord-0ad487086dea4a00aeb59f61f85a9439 |
| 出典メモ | uspto-grants-1991_05 |