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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626775Generated: November 2, 2026

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

https://huagongshe.com/reaction/1626775

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(cyanomethylidene)piperidine-1-carboxylateHCID 15326949—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(cyanomethyl)piperidine-1-carboxylateHCID 22248390112.7%

Reaction Steps

tert-Butyl 4-(cyanomethylene)piperidine-1-carboxylate (20 g, 91 mmol) was dissolved in ethyl acetate (400 mL), and 10% palladium-activated carbon (3.0 g) was added, followed by stirring at room temperature for 3.5 hours under a hydrogen atmosphere. The reaction solution was filtered with celite, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by chromatography on a silica gel column (Moritex Corporation, elution solvent: hexane/ethyl acetate), and a fraction corresponding to the Rf value=0.38 (hexane/ethyl acetate=3/1) by thin layer chromatography was concentrated under reduced pressure to afford the title compound (23 g) as a white solid (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785462B2
Source datasetuspto-grants-2014_07
ORD IDord-0aba60d12cc34640848f0377f15b999e
Source noteuspto-grants-2014_07