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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035307Generated: October 30, 2026

Water → 1-Methoxypiperidine-4-carbonitrile

https://huagongshe.com/reaction/2035307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanesulfonic acid 1-methoxy-piperidin-4-yl esterHCID 86663299—
CatalystTetrabutylammonium CyanideHCID 165872—
SolventDimethyl SulfoxideHCID 679—
Product1-Methoxypiperidine-4-carbonitrileHCID 6679397086.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

200 mg Methanesulfonic acid 1-methoxy-piperidin-4-yl ester (from Step 2), 251 mg tetrabutylammonium cyanide and 272 mg sodium cyanide were mixed in 1 ml dimethylsulfoxide, and heated to 55° C. for 18 hours. Then the mixture was cooled to room temperature, 1 ml saturated aqueous sodium bicarbonate and 3 ml water were added, and extracted three times with diethyl ether. The organic layer was dried over anhydrous sodium sulfate and the solvent evaporated. The residue was purified by chromatography on silica gel with ethyl acetate/cyclohexane (1:1, then 2:1, then pure ethyl acetate) as a solvent. 116 mg 1-methoxy-piperidine-4-carbonitrile was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08574607B2
Source datasetuspto-grants-2013_11
ORD IDord-979cb16aaf744ea7aa02586e523dc5eb
Source noteuspto-grants-2013_11