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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461244Generated: November 2, 2026

Hydroxyamine hydrochloride → 6-Hydroxymethyl-5-p-methoxybenzyloxy-2-methyl-1-hydroxy-4-pyridone

https://huagongshe.com/reaction/1461244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant6-Hydroxymethyl-5-p-methoxybenzyloxy-2-methyl-4-pyroneHCID 14652926—
SolventPyridineHCID 1049—
Product6-Hydroxymethyl-5-p-methoxybenzyloxy-2-methyl-1-hydroxy-4-pyridoneHCID 146529278.3%

Reaction Steps

To a solution of 4 g of 6-hydroxymethyl-5-p-methoxybenzyloxy-2-methyl-4-pyrone in 50 ml of pyridine was added 5 g of hydroxylamine hydrochloride at room temperature. The mixture was stirred at 70° to 75° C. for 7 hours. After the reaction liquid was concentrated under reduced pressure, the residue was dissolved in 200 ml of chloroform and washed in succession with water, 5% cold hydrochloric acid and saturated aqueous sodium hydrogencarbonate solution. After drying over anhydrous magnesium sulfate, the chloroform layer was dried and concentrated under reduced pressure. The concentrate was separated and purified by flash column chromatography (eluting solution; chloroform: methanol=20:1) using Wako Gel C-300 (100 g) to give 350 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075299
Source datasetuspto-grants-1991_12
ORD IDord-f2636cc723764fb59f5c97ceefde2992
Source noteuspto-grants-1991_12