Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218403Generated: October 29, 2026

(R)-tert-butyl 3-((R)-(2-azidoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylate → (R)-tert-butyl 3-((R)-(2-aminoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/218403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-butyl 3-((R)-(2-azidoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylateHCID 58011545—
CatalystPalladium hydroxideHCID 9942167—
SolventEthyl AcetateHCID 8857—
Product(R)-tert-butyl 3-((R)-(2-aminoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylateHCID 5801152894.7%

Reaction Steps

(R)-tert-butyl 3-((R)-(2-azidoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylate (7 g, 17.1 mmol.) was dissolved in EtOAc (300 mL), 0.8 g of Pd(OH)2 was added and the air in bottle was replaced 3 times with H2, the reaction was stirred at rt for 3 hr. The solution was filtered and concentrated to give (R)-tert-butyl 3-((R)-(2-aminoethoxy)(5-chloro-2-methylphenyl)methyl)piperidine-1-carboxylate (6.2 g), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198453B2
Source datasetuspto-grants-2012_06
ORD IDord-6a9a99f62da44ec19be2e5eaa9506c0c
Source noteuspto-grants-2012_06