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HRID 400067作成日:2026年10月27日

Sodium Hydroxide → 1-Benzyl-4-(pyridin-2-yl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/400067

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Pyridine-2-acetonitrileHCID 75959—
反応物N,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
触媒Hexadecyltributylphosphonium bromideHCID 84716—
生成物1-Benzyl-4-(pyridin-2-yl)piperidine-4-carbonitrileHCID 22725232—

反応条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05824690
出典データセットuspto-grants-1998_10
ORD IDord-296e5b50ac0e45a9bc4bd1d70f9752af
出典メモuspto-grants-1998_10