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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616075Generated: November 1, 2026

Water → tert-Butyl 4-(cyanomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1616075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
ReactantTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—
SolventEthanolHCID 702—
Producttert-Butyl 4-(cyanomethyl)piperidine-1-carboxylateHCID 2224839077%

Reaction Steps

tert-Butyl 4-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate (15.3 g) was dissolved in ethanol (80 mL), water (20 mL) and sodium cyanide (4.0 g, 80 mmol) were added, and stirring was conducted at 80° C. for 24 hours. Ethanol was distilled off, water and ethyl acetate were added, and then the resultant mixture was subject to Celite filtration, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under a reduced pressure, and the obtained residue was purified by using silica gel column chromatography (hexane:ethyl acetate=3:1→2:1) to give tert-butyl 4-(cyanomethyl)piperidine-1-carboxylate (6.87 g, 77%, 3 steps) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765771B2
Source datasetuspto-grants-2014_07
ORD IDord-4a8eef4698b24512b037e2164243767f
Source noteuspto-grants-2014_07