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HRID 343497Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/343497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhenylacetonitrileHCID 8794—
EduktPotassium HydroxideHCID 14797—
EduktSodium HydroxideHCID 14798—
EduktN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
EduktTriethyl(hexadecyl)phosphanium bromideHCID 21951238—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-Piperidinecarbonitrile, 4-phenyl-1-(phenylmethyl)-, hydrochloride (1:1)HCID 12652062—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861417
Quelldatensatzuspto-grants-1999_01
ORD IDord-f7969df0790a4ae481bb3fbccad1625b
Quellennotizuspto-grants-1999_01