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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1022369Erstellt: 26. Oktober 2026

Sodium Cyanide → 4-Amino-1-methoxy-piperidine-4-carbonitrile

https://huagongshe.com/reaction/1022369

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CyanideHCID 8929—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Methoxypiperidin-4-oneHCID 19936653—
LösungsmittelWaterHCID 962—
LösungsmittelAmmonium HydroxideHCID 14923—
Produkt4-Amino-1-methoxy-piperidine-4-carbonitrileHCID 5961459468,7%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To 10 g of N-methoxy-4-piperidone (J. Org. Chem. 1961, 26, 1867-74) in 240 ml ammoniumhydroxide 25% in water there are added 6.2 g of ammoniumchloride and 4.6 g of sodium cyanide. After stirring for 18 h at 25° C. the reaction mixture is diluted with 200 ml water and extracted with ethyl acetate. The organic phase is separated, dried over sodium sulphate, filtered and evaporated. 8.25 g of 4-amino-1-methoxy-piperidine-4-carbonitrile is obtained as light brow oil, which is used without further purification in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722578B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-f4e338df5ee04a02bd6e4dab3868329c
Quellennotizuspto-grants-2014_05