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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986186Generated: October 26, 2026

Ammonia → Tert-butyl 4-(3-aminopropyl)-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1986186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttrans-4-(2-Cyanovinyl)-4-methylpiperidine-1-carboxylic acid tert-butyl esterHCID 68857538—
ReactantHCID 178418361HCID 178418361—
CatalystRhodiumHCID 23948—
SolventEthanolHCID 702—
ProductTert-butyl 4-(3-aminopropyl)-4-methylpiperidine-1-carboxylateHCID 6885705563.4%

Reaction Steps

Cis/trans-4-(2-cyanovinyl)-4-methylpiperidine-1-carboxylic acid tert-butyl ester (1.00 g, 4.0 mmol), 5% Rh/Al2O3 (0.500 g) and 28% aqueous NH3 (1.25 mL) are heated at 35° C. in ethanol (20 mL) and 50 psi hydrogen gas for 18 hours. The reaction mixture is filtered through Celite®, concentrated, and chromatographed with 0-20% (2M NH3 in MeOH) in dichloromethane to give the title compound as a clear oil (0.65 g, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-8b342d06199d4a3c875f8672994238f5
Source noteuspto-grants-2009_06