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HRID 343497作成日:2026年10月26日

Hydrochloric Acid → 4-Piperidinecarbonitrile, 4-phenyl-1-(phenylmethyl)-, hydrochloride (1:1)

https://huagongshe.com/reaction/343497

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物PhenylacetonitrileHCID 8794—
反応物Potassium HydroxideHCID 14797—
反応物Sodium HydroxideHCID 14798—
反応物N,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
反応物Triethyl(hexadecyl)phosphanium bromideHCID 21951238—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物4-Piperidinecarbonitrile, 4-phenyl-1-(phenylmethyl)-, hydrochloride (1:1)HCID 12652062—

反応条件

温度100 °C

反応手順

Combine phenylacetonitrile (40 mmol), and aqueous sodium hydroxide solution (60 mL, 50% by weight). Add N,N-bis(2-chloroethyl)benzylamine hydrochloric acid salt (11.28 g, 42 mmol) and hexadecyltriethyl phosphonium bromide (1.02 g, 2 mmol). Heat to 100° C and stir vigorously. After 1 hour, cool the reaction mixture to ambient temperature. Add water and acidify the diluted reaction mixture with an aqueous 6M hydrochloric acid solution. Extract the acidified reaction mixture with diethyl ether. Adjust the pH of the aqueous layer to about 12 using solid potassium hydroxide and extract with ethyl acetate. Separate the ethyl acetate layer, dry over MgSO4, filter, and evaporate invacuo to give a residue. Combine the residue and a solution of hydrochloric acid in methanol. Evaporate in vacuo to give 1-benzyl-4-phenyl-4-cyanopiperidine hydrochloric acid salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861417
出典データセットuspto-grants-1999_01
ORD IDord-f7969df0790a4ae481bb3fbccad1625b
出典メモuspto-grants-1999_01