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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352748Generated: October 30, 2026

Tert-butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate → tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/352748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 10377658—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Producttert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylateHCID 1514280—

Reaction Steps

In ethanol (10 ml), 1-tert-butoxycarbonyl-4-[(methoxycarbonyl)methylene]piperidine (875 mg) was dissolved, followed by the addition of 10% palladium carbon (water content: about 50%, 730 mg). The resulting mixture was subjected to catalytic hydrogenation under normal pressure at room temperature for 3 days. After the removal of the catalyst by filtration, the solvent was distilled off under reduced pressure, whereby the title compound (871 mg, 99%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-9a1d9278bbdb4550bb4105e6035cd81d
Source noteuspto-grants-2004_06