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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695883Generated: November 1, 2026

tert-Butyl 4-{[(2-nitrophenyl)methyl]amino}piperidine-1-carboxylate → tert-Butyl 4-(2-aminobenzylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1695883

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-{[(2-nitrophenyl)methyl]amino}piperidine-1-carboxylateHCID 13046886—
SolventMethanolHCID 887—
Producttert-Butyl 4-(2-aminobenzylamino)piperidine-1-carboxylateHCID 13046887—

Reaction Steps

A solution of tert-Butyl 4-(2-nitrobenzylamino)piperidine-1-carboxylate (24 g, 71.6 mmol) in MeOH (150 ml) was stirred under an atmosphere of hydrogen for 24 hours. The reaction mixture was filtered and evaporated to give the crude amine, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-22a73667be504c1892a66a69daf77d1a
Source noteuspto-grants-2012_04