化工社化工社 化学情報印刷レポート · 研究参考用
Ammonium Acetate → 1-[(4-Methylphenyl)methyl]piperidin-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | 1-(4-Methylbenzyl)piperidin-4-one | HCID 11959541 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-[(4-Methylphenyl)methyl]piperidin-4-amine | HCID 12641836 | 48.9% |
反応手順
To 4.25 g (21 mmol) of 1-(4-methylbenzyl)-4-piperidinone 124 in 200 mL of anhydrous methanol was added 32.2 g (420 mmol) of ammonium acetate and 25 g of 3A molecular sieves. After stirring 30 min, 5.25 g (84 mmol) of sodium cyanoborohydride was added portionwise. After stirring 16 hours, the mixture was gravity filtered and the methanol evaporated under vacuum. The residue was partitioned between ether and ice/HCl. The acidic aqueous layer was extracted twice with ether, made basic with 50% aqueous NaOH and ice, and extracted with CH2Cl2 to give 2.1 g (48%) of the title amine 125 as a thick oil. GC/MS showed a molecular ion of 204. The product was used as is without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706740B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-9bf5a068f7d446908f3027c600854fa9 |
| 出典メモ | uspto-grants-2004_03 |