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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044403Generated: October 30, 2026

4-(benzyloxy)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one → 4-hydroxy-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1044403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(benzyloxy)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-oneHCID 58580264—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-hydroxy-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-oneHCID 5858029398%

Reaction Steps

A mixture of 4-(benzyloxy)-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one Part B (287 mg, 0.73 mmol) and 10% Pd/C (7.72 mg, 0.073 mmol) in MeOH (15 mL) was hydrogenated at 50 PSI of H2 for 4 hours. Pd/C was filtered off and the filtrate was concentrated giving 4-hydroxy-1-(4-(2-hydroxy-2-methylpropoxy)-3-methoxyphenyl)pyridin-2(1H)-one 7C (228 mg, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563583B2
Source datasetuspto-grants-2013_10
ORD IDord-7c1a325aab9b4796a11d545cc0f8728a
Source noteuspto-grants-2013_10