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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795169Generated: November 2, 2026

4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl ester → 4-Cyclohexyl-4-(2-methoxycarbonylethyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1795169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 69597110—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Cyclohexyl-4-(2-methoxycarbonylethyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 2338869797%

Reaction Steps

To a solution of 4-cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl ester, 8, (2.64 g, 7.5 mmole) in methanol (30 ml) is added 10% palladium on carbon (120 mg) under argon. The mixture is purged with hydrogen and then stirred for two hours under a hydrogen atmosphere at atmospheric pressure. The reaction mixture is filtered through a short pad of Celite and the filtrate concentrated under reduced pressure. The crude product is purified over silica to afford 2.57 g (97% yield) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026335B2
Source datasetuspto-grants-2006_04
ORD IDord-8f83c134885c4f5ab4d7d022b1ae5384
Source noteuspto-grants-2006_04