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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594368Generated: November 2, 2026

1-(4-(Benzyloxy)benzyl)-6-(2,6-dimethoxyphenyl)piperidin-2-one → 6-(2,6-Dimethoxyphenyl)-1-(4-hydroxybenzyl)piperidin-2-one

https://huagongshe.com/reaction/594368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(Benzyloxy)benzyl)-6-(2,6-dimethoxyphenyl)piperidin-2-oneHCID 69081351—
SolventEthanolHCID 702—
Product6-(2,6-Dimethoxyphenyl)-1-(4-hydroxybenzyl)piperidin-2-oneHCID 69081744—

Reaction Steps

A mixture of 1-(4-(benzyloxy)benzyl)-6-(2,6-dimethoxyphenyl)piperidin-2-one (74 mg; 0.17 mmol), and 10% Pd(C) (35 mg) in anh. EtOH (3 ml) was stirred at rt, under hydrogen atmosphere (1 atm), for 15 h. Filtration over a pad of celite, concentration to dryness under reduced pressure, and additional drying under HV afforded 6-(2,6-dimethoxyphenyl)-1-(4-hydroxybenzyl)piperidin-2-one as a yellow oil. LC-MS (conditions E): tR=0.62 min.; [M+H]+: 342.20 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-22c71af979344fba8eeeb2bf0df19e3d
Source noteuspto-grants-2016_01