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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695888Generated: November 4, 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/1695888

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 numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-c72819f9aeaa4d11abbc46fa451a4be9
Source noteuspto-grants-2012_04