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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056901Generated: October 27, 2026

Water → 1-(3-bromophenyl)-2-hydroxymethyl-5-(4-methoxy-benzyloxy)-1H-pyridin-4-one

https://huagongshe.com/reaction/1056901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant1-(3-bromophenyl)-5-hydroxy-2-(hydroxymethyl)pyridin-4(1H)-oneHCID 67408533—
SolventDimethylformamideHCID 6228—
Product1-(3-bromophenyl)-2-hydroxymethyl-5-(4-methoxy-benzyloxy)-1H-pyridin-4-oneHCID 67417962—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 1-(3-bromo-phenyl)-5-hydroxy-2-hydroxymethyl-1H-pyridin-4-one and K2CO3 (5.17 g, 37.5 mmol) in 50 mL of DMF was added 2.35 g of PMBCl (15 mmol) dropwise, and the reaction mixture was stirred at 80° C. for 3 h. After cooling to room temperature, the mixture was poured into 200 mL of water and extracted with EtOAc (50 mL) three times. The combined organic layers were washed with water, brine, and dried over anhydrous MgSO4. Most of the volatiies were removed in vacuo and the resulting solid was collected and washed with EtOAc to obtain 1-(3-bromophenyl)-2-hydroxymethyl-5-(4-methoxy-benzyloxy)-1H-pyridin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399651B2
Source datasetuspto-grants-2016_07
ORD IDord-54768563ff34401f89dfff6c7fc3bd79
Source noteuspto-grants-2016_07