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HRID 343497생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/343497

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhenylacetonitrileHCID 8794—
반응물Potassium HydroxideHCID 14797—
반응물Sodium HydroxideHCID 14798—
반응물N,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
반응물Triethyl(hexadecyl)phosphanium bromideHCID 21951238—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-Piperidinecarbonitrile, 4-phenyl-1-(phenylmethyl)-, hydrochloride (1:1)HCID 12652062—

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861417
출처 데이터셋uspto-grants-1999_01
ORD IDord-f7969df0790a4ae481bb3fbccad1625b
출처 메모uspto-grants-1999_01