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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658352Generated: October 28, 2026

Hydrogen Peroxide → HCID 178481654, compound

https://huagongshe.com/reaction/658352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethanolHCID 887—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 178503198HCID 178503198—
CatalystSodium tungstateHCID 26052—
ProductHCID 178481654HCID 17848165429%
ProductHCID 178481655HCID 17848165512%

Reaction Steps

2-[1,2-dihydro-1-methyl-6-methylthio-2-oxopyridine-3-carbonyl]-3-hydroxy-2-cyclohexen-1-one (1.2 g, 4.1 mmol), sodium tungstate (0.13 g, 0.4 mmol) and aqueous 35% hydrogen peroxide (0.48 g, 5.4 mmol) were dissolved in methanol (2 mL), and the mixture was stirred for 5 hours at room temperature. The mixed solution was poured into a sodium hydrogensulfite solution, and extracted with chloroform. The obtained organic layer was dried over anhydrous magnesium sulfate, the inorganic substance was separated by filtration, and then the solvent was distilled off under reduced pressure. Thus obtained residue was purified by column chromatography to obtain 0.36 g of 2-[1,2-dihydro-1-methyl-6-methylsulfinyl-2-oxopyridine-3-carbonyl]-3-hydroxy-2-cyclohexen-1-one (1.2 mmol, yield: 29%) and 0.16 g of 2-[1,2-dihydro-1-methyl-6-methylsulfonyl-2-oxopyridine-3-carbonyl]-3-hydroxy-2-cyclohexen-1-one (0.49 mmol, yield: 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076487B2
Source datasetuspto-grants-2011_12
ORD IDord-dca05356349d4bf2b981a4ef98f4a9ea
Source noteuspto-grants-2011_12