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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187470Generated: October 25, 2026

5-(benzyloxy)-2-methylpyridin-4(1H)-one → 5-hydroxy-2-methylpyridin-4(1H)-one

https://huagongshe.com/reaction/1187470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(benzyloxy)-2-methylpyridin-4(1H)-oneHCID 6324719—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-hydroxy-2-methylpyridin-4(1H)-oneHCID 64264970.5%

Reaction Steps

A solution of 5-benzyloxy-2-methyl-1H-pyridin-4-one (2 g, 9.29 mmol) in methanol (30 ml) and water (8 ml) was placed in a Parr bottle. 10% Pd/C was added and the mixture was hydrogenated at 50 psi for 3 hours. A bed of CELITE™ was placed on a sintered glass, and washed with 0.1N HCl and then water. The content in the Parr bottle was removed from the Parr hydrogenator and flushed with nitrogen. The solution was filtered under suction. The filtrate was evaporated to give a white solid (820 mg, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673943B2
Source datasetuspto-grants-2014_03
ORD IDord-2b44199cd4514f1d851c7ec6e91eaf55
Source noteuspto-grants-2014_03