化工社化工社化学信息打印报告 · 仅供科研参考
2-氯吡啶 → (R)-N-(2-pyridyl)-2-aminopropanol
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 2-氯吡啶 | HCID 7977 | — |
| 反应物 | D-氨基丙醇 | HCID 80308 | — |
| 反应物 | 叔丁醇钾 | HCID 23665647 | — |
| 溶剂 | 四氢呋喃 | HCID 8028 | — |
| 产物 | (R)-N-(2-pyridyl)-2-aminopropanol | HCID 21339422 | 87.4% |
反应步骤
(R)-Alaninol (107.3 g, 1.43M) was added dropwise with stirring to a solution of potassium tertiary butoxide (160 g, 1.43M) in tetrahydrofuran (1L). After the exothermic reaction had cooled to room termperature, 2-chloropyridine (162.4 g, 1.43M) was added dropwise. The reaction mixture was heated under reflux overnight, cooled, filtered and evaporated to an oil. The oil was dissolved in xylene (1,5L) and toluene-p-sulphonic acid (0.5 g) was added. The mixture was heated under reflux overnight. On cooling to room temperature the product crystallised to give (R)-N-(2-pyridyl)-2-aminopropanol (190 g), [α]D26=30° (c=1 in CHCl3).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US06395902B1 |
| 来源数据集 | uspto-grants-2002_05 |
| ORD ID | ord-567d0f352f694ca785f48c23cb95f136 |
| 来源说明 | uspto-grants-2002_05 |