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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039918Generated: November 1, 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/2039918

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 5801152894.6%

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 numberUS08580823B2
Source datasetuspto-grants-2013_11
ORD IDord-a81e6e28b1bd4452b354798f40158f93
Source noteuspto-grants-2013_11