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Ammonia → Tert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Tert-butyl 4-(cyano(phenyl)methylene)piperidine-1-carboxylate | HCID 44122578 | — |
| 触媒 | Nickel | HCID 935 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Tert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylate | HCID 58415947 | — |
反応手順
tert-butyl 4-[cyano(phenyl)methylene]piperidine-1-carboxylate (1.18 g, 3.95 mmol) in ethanol (15 ml) was saturated with NH3 at ambient temperature and Raney nickel (1 ml, 3.95 mmol) in water was added. The reaction was placed on a Parr reactor under H2 pressure (48 psi) for 19 hours. The reaction mixture was then re-saturated with NH3 and additional Raney nickel (1 ml, 3.95 mmol) was added before placing back on the Parr reactor for an additional 5.5 hours. The reaction mixture was filtered through Celite, washing with EtOH, and concentrated in vacuo. The product was carried on without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08389720B2 |
| 出典データセット | uspto-grants-2013_03 |
| ORD ID | ord-ab0346fb6807451ebe1ee52b8b17c723 |
| 出典メモ | uspto-grants-2013_03 |