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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017546Generated: October 30, 2026

Sodium Cyanide → Ethyl 4-(3-cyanopropyl)-4-cyano-1-piperidinecarboxylate

https://huagongshe.com/reaction/1017546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantEthyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylateHCID 9838044—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(3-cyanopropyl)-4-cyano-1-piperidinecarboxylateHCID 1019884588.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of ethyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylate (12.7 g) in dimethylformamide (250 ml) was added sodium cyanide (24 g) under nitrogen, with stirring. The mixture was warmed at 140° C. overnight and then cooled to ambient temperature, diluted with water and extracted with ethyl acetate. The organic extracts were washed with saturated, sodium chloride solution and water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was chromatographed, eluting with 2:1 heptane/ethyl acetate. The appropriate fractions were collected and concentrated to give 10.8 g (88.5%) of product. A portion was distilled to give the analytical sample, bp 196-201° C. (4 mm of mercury).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479501B2
Source datasetuspto-grants-2002_11
ORD IDord-07de8a92a23e43a2863ecaaa92e147dc
Source noteuspto-grants-2002_11