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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218506Generated: October 30, 2026

3-Methoxy-2-pyridone → HCID 59586725, compound

https://huagongshe.com/reaction/218506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-pyridoneHCID 88731—
Reactant2-(Difluoromethoxy)-1-fluoro-4-nitro-benzeneHCID 20131434—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductHCID 59586725HCID 59586725—

Reaction Conditions

Temperature80 °C

Reaction Steps

302 mg (2.41 mmol) of 3-methoxypyridone are dissolved in 8.2 ml of anhydrous dimethyl sulfoxide and admixed with 325 mg (2.89 mmol) of potassium tert-butoxide. After 30 min, 500 mg (2.41 mmol) of 2-(difluoromethoxy)-1-fluoro-4-nitrobenzene are added and the mixture is heated to 80° C. for 20 h. The reaction solution is diluted with dichloromethane and washed with water and 1N hydrochloric acid. After the organic phase has been dried over sodium sulfate, it is filtered and concentrated to dryness under reduced pressure. The residue is dissolved in dimethyl sulfoxide and purified by preparative HPLC with a water/acetonitrile gradient. The product fractions are combined and concentrated to dryness under reduced pressure. This affords 207 mg (28% of theory) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198267B2
Source datasetuspto-grants-2012_06
ORD IDord-613ac57eb69c41b59e8642ec5330dd1f
Source noteuspto-grants-2012_06