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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172289Generated: October 31, 2026

tert-Butyl 4-{[2-(2-nitrophenyl)ethyl]amino}piperidine-1-carboxylate → Tert-butyl 4-{[2-(2-aminophenyl)ethyl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/1172289

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-{[2-(2-nitrophenyl)ethyl]amino}piperidine-1-carboxylateHCID 18444265—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl 4-{[2-(2-aminophenyl)ethyl]amino}piperidine-1-carboxylateHCID 18444264100%

Reaction Steps

To a solution of tert-butyl 4-(2-nitrophenethylamino)piperidine-1-carboxylate (10.5 g) in EtOH (180 ml) was added 10% Pd/C (1.05 g) and the reaction mixture was stirred at RT under an atmosphere of H2 overnight. The reaction mixture was filtered and the resulting solution was evaporated to dryness giving the desired product (9.6 g). LC/MS (10% to 99%): M/Z (M+H)+ (obs)=320; tR=2.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834000B2
Source datasetuspto-grants-2010_11
ORD IDord-4acb313dfdc043ffb17cd0ee9dd833dc
Source noteuspto-grants-2010_11