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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627113Generated: October 29, 2026

Hydrochloric Acid → 6-Hydroxymethyl-3,4-bis[(p-methoxybenzyl)oxy]-pyridine

https://huagongshe.com/reaction/627113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant2-(Hydroxymethyl)-5-[(4-methoxyphenyl)methoxy]pyridin-4(1H)-oneHCID 15159532—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Hydroxymethyl-3,4-bis[(p-methoxybenzyl)oxy]-pyridineHCID 1566250652%

Reaction Steps

To a solution of 2-(hydroxymethyl)-5-(4-methoxybenzyloxy)pyridin-4(1H)-one (Intermediate 62, 3.48 g, 13.32 mmol) in DMF (100 mL) at room temperature was added 4-methoxybenzyl chloride (1.987 mL, 14.65 mmol) followed by potassium carbonate (2.273 mL, 39.96 mmol). The reaction mixture was stirred for 1 hour at room temperature then heated at 80° C. for 1.5 hours. The reaction mixture was cooled to room temperature, poured into water and extracted twice with ethyl acetate. The combined extracts were washed with water and brine. The ethyl acetate layer was concentrated to afford an oil. To the oil was added 1N HCl and a light brown solid crashed out. This was collected by filtration. The solid was taken up in ethyl acetate and washed with saturated sodium bicarbonate. The organics were dried over magnesium sulfate, filtered and concentrated to afford the title compound as a brown solid (2.62 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-a3a171704dc8425e8667644eb6c46fbf
Source noteuspto-grants-2016_04