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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603200Generated: November 1, 2026

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

https://huagongshe.com/reaction/1603200

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, bp196-201° C. (4 mm of mercury).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05986097
Source datasetuspto-grants-1999_11
ORD IDord-7290891dbc1b4cbdb369cd71e3d9014f
Source noteuspto-grants-1999_11