化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → 4-[(Piperidin-4-yl)methyl]aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-(4-Nitrobenzyl)pyridine | HCID 14129 | — |
| 触媒 | Adams' catalyst | HCID 345198 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-[(Piperidin-4-yl)methyl]aniline | HCID 10997824 | 86.3% |
反応手順
A mixture of 4-(4-nitrobenzyl)pyridine (12.85 g, 60 mmol), platinum(IV) oxide (1.0 g), 12N hydrochloric acid (5 ml, 60 mmol), water (5 ml) in ethanol (200 ml) was hydrogenated at 40 psi in a Parr apparatus for 12 hours. The reaction mixture was concentrated in vacuo, and the residue was diluted with cold water and basified with 10% sodium hydroxide solution. The resulting mixture was extracted into ethyl acetate. The combined organic extracts were washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The residue on crystallization from ethyl acetate/hexanes gave 4-(piperidin-4-ylmethyl)-phenylamine (9.85 g, 86%) as a white crystalline solid, m.p. 110-113° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06184242B2 |
| 出典データセット | uspto-grants-2001_02 |
| ORD ID | ord-1c56253fd1cd4e318801626525f419b7 |
| 出典メモ | uspto-grants-2001_02 |