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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262312Generated: November 2, 2026

1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-ol → 1-[(4-Amino-3-methoxyphenyl)methyl]piperidin-4-ol

https://huagongshe.com/reaction/1262312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-olHCID 66711686—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-[(4-Amino-3-methoxyphenyl)methyl]piperidin-4-olHCID 57416113—

Reaction Steps

Into a par bottle, 1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-ol (0.74 g, 2.8 mmol), Ethanol (20 mL) and 10% Pd/C (10:90, Palladium:carbon black, 0.30 g, 0.28 mmol) were added. The reaction mixture was evacuated and charged with hydrogen at 35 psi. The mixture was shaken for 3 hours. The solid was filtered through Celite and washed with methanol. The solvent was removed under vacuum to give 1-(4-Amino-3-methoxy-benzyl)-piperidin-4-ol as a semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-042736b39a7540b09872451e76173697
Source noteuspto-grants-2013_06