関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Pyridine-2-acetonitrile | HCID 75959 | — |
| 反応物 | N,N-Bis(2-chloroethyl)benzylamine hydrochloride | HCID 2777881 | — |
| 触媒 | Hexadecyltributylphosphonium bromide | HCID 84716 | — |
| 生成物 | 1-Benzyl-4-(pyridin-2-yl)piperidine-4-carbonitrile | HCID 22725232 | — |
反応手順
Combine 2-pyridylacetonitrile (5.9 g, 50 mmol), N-benzyl-N,N-bis-(2-chloroethyl)amine hydrochloride (13.4 g, 50 mmol), and hexadecyltributyphosphonium bromide (1.3 g, 2.5 mmol) and a 50% aqueous sodium hydroxide solution (75 mL). Heat to 100° C. After 1 hour, cool the reaction mixture to ambient temperature and repeatedly extract with diethyl ether. Extract the combined organic layers twice with an aqueous 10% hydrochloric acid solution (350 mL). combine the aqueous layers and neutralize with an aqueous 50% sodium hydroxide solution. Again extract three times with diethyl ether, combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give 1-benzyl-4-cyano-4-(pyridin-2-yl)-piperidine: Rf =0.56 (silica gel, 9/1 dichloromethane/methanol). Elemental Analysis calculated for C18 H19N3 : C, 77.95; H, 6.90; N, 15.15. Found: C, 78.20; H, 6.97; N, 15.04.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05824690 |
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| 出典データセット | uspto-grants-1998_10 |
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| ORD ID | ord-296e5b50ac0e45a9bc4bd1d70f9752af |
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| 出典メモ | uspto-grants-1998_10 |
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