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1-(3,4-Dichlorobenzyl)-4-(2-nitrocyclohexyl)piperazine → 1-(3,4-Dichlorobenzyl)-4-(2-aminocyclohexyl)piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(3,4-Dichlorobenzyl)-4-(2-nitrocyclohexyl)piperazine | HCID 22257751 | — |
| 触媒 | Adams' catalyst | HCID 345198 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 1-(3,4-Dichlorobenzyl)-4-(2-aminocyclohexyl)piperazine | HCID 22257736 | 69.5% |
反応手順
Platinum (IV) oxide (15 mg, 0.07 mmol) was added to a solution of 1-(3,4-dichlorobenzyl)-4-(2-nitrocyclohexyl)piperazine (187 mg, 0.50 mmol) in glacial acetic acid (5 ml). The reaction mixture was stirred under hydrogen atmosphere at room temperature for 16 h. The reaction mixture was then filtered through a pad of celite. The filtrate was made basic with a 15% sodium hydroxide solution and the product was extracted into ethyl acetate. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to provide 1-(3,4-dichlorobenzyl)-4-(2-aminocyclohexyl)-piperazine (119 mg) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06323223B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-bf195f8d8c7042a085497658d15b11d9 |
| 出典メモ | uspto-grants-2001_11 |