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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242819Generated: October 25, 2026

(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester → (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester

https://huagongshe.com/reaction/242819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 59073577—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 59918925—

Reaction Steps

A mixture of (R)-3-(2-nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester (2.48 g, 7.72 mmol) and 10% Pd/C (250 mg) in EtOAc (50 mL) was degassed with a stream of nitrogen and stirred at RT under a hydrogen atmosphere for 20 h. The suspension was then filtered through a PTFE frit and the filtrate was concentrated in vacuo affording (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester as a clear glass (2.25 g, quantitative). LCMS: RT 2.64 min [M+H-Boc]+ 192.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-782192cd7b5c42ae8147566990c677f8
Source noteuspto-grants-2014_02