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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625972Generated: October 30, 2026

3-(benzyloxy)-5-(biphenyl-3-yl)-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-one → 5-(biphenyl-3-yl)-3-hydroxy-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/625972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(benzyloxy)-5-(biphenyl-3-yl)-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-oneHCID 71149956—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-(biphenyl-3-yl)-3-hydroxy-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-oneHCID 5337990631.2%

Reaction Steps

To a solution of 3-(benzyloxy)-5-(biphenyl-3-yl)-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-one (100 mg, 0.205 mmol) in 5 mL methanol, was added 10% palladium on charcoal (21.83 mg, 0.02 mmol). The resulting mixture was stirred at room temperature under hydrogen (1 atm) for 45 min. The mixture was filtered to remove charcoal, concentrated and purified by reversed-phase HPLC to afford 5-(biphenyl-3-yl)-3-hydroxy-6-(1-hydroxy-2-phenylethyl)-1-methylpyridin-2(1H)-one (25.4 mg, 0.064 mmol, 31.2% yield). ES-MS (M+H)+=398. High resolution mass spec (ESI) calc (M+H)+=398.1751 found 398.1754

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309199B2
Source datasetuspto-grants-2016_04
ORD IDord-7e548fa82c0640808b5745be5713ce8d
Source noteuspto-grants-2016_04