Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609807Generated: October 30, 2026

HCID 69352738, compound → HCID 69351642, compound

https://huagongshe.com/reaction/1609807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69352738HCID 69352738—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 69351642HCID 6935164288%

Reaction Steps

A mixture of 1-benzyl-(3S)-3-(4-nitrophenoxy)piperidine (6.5 g) and 1.2 g of 10% Pd/C in methanol (30 mL) was subjected to hydrogenation (50 psi). When the reaction was completed, the reaction mixture was filtered. The filtrate was concentrated in vacuo, giving a yellow solid. Recrystallization in CH2Cl2/hexane afforded (3S)-3-(4-aminophenoxy)piperidine (3.5 g, 88% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982259B2
Source datasetuspto-grants-2006_01
ORD IDord-4a5277ee83574ceaba841b2fb2b03de7
Source noteuspto-grants-2006_01