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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022369Generated: October 25, 2026

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

https://huagongshe.com/reaction/1022369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Methoxypiperidin-4-oneHCID 19936653—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
Product4-Amino-1-methoxy-piperidine-4-carbonitrileHCID 5961459468.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722578B2
Source datasetuspto-grants-2014_05
ORD IDord-f4e338df5ee04a02bd6e4dab3868329c
Source noteuspto-grants-2014_05