Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795175Generated: October 30, 2026

Ammonia → 4-(3-Aminopropyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1795175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-(2-Cyanovinyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl esterHCID 69597086—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product4-(3-Aminopropyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl esterHCID 21023774—

Reaction Steps

To a solution of 4-(2-cyanovinyl)-4-cyclohexylpiperidine-1-carboxylic acid tert-butyl ester, 14, (800 mg, 2.35 mmol) in MeOH (33 mL) is added ammonia (16 mL) and Raney Ni (50 mg). The reaction mixture is degassed with nitrogen, purged with hydrogen gas and shaken under an atmosphere of hydrogen (45 psi) on a standard hydrogenation apparatus at room temperature for 6 hours. The reaction solution is filtered to remove the catalyst and the solvent removed in vacuo to afford the desired product was obtained as a colorless, sticky oil in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026335B2
Source datasetuspto-grants-2006_04
ORD IDord-6d37f3a415b64af89315f71cd3701724
Source noteuspto-grants-2006_04