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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802330Generated: November 1, 2026

Potassium Bicarbonate → 5-(2,6-Difluorophenyl)-N,N-dimethyl-4,5-dihydroisoxazole-3-carboxamide

https://huagongshe.com/reaction/1802330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
Reactant2,6-DifluorostyreneHCID 2778300—
ReactantEthanimidoyl chloride, 2-(dimethylamino)-N-hydroxy-2-oxo-HCID 53423335—
SolventWaterHCID 962—
SolventChlorobenzeneHCID 7964—
Product5-(2,6-Difluorophenyl)-N,N-dimethyl-4,5-dihydroisoxazole-3-carboxamideHCID 66618229—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a 1000-mL round bottom flask equipped with a mechanical stirrer, thermometer and addition funnel were added 2-(dimethylamino)-N-hydroxy-2-oxoethanimidoyl chloride (94.0 g, 0.62 mol) and a solution of 2,6-difluorostyrene (84.0 g, 0.60 mol) in chlorobenzene (275 g). The reaction mixture was cooled to 10° C., and then a solution of potassium bicarbonate (70 g, 0.70 mol) in water (350 mL) was added dropwise over 1 h while maintaining the temperature between 10 to 15° C. When gas chromatography analysis of the reaction mixture showed about 3% of 2-(dimethylamino)-N-hydroxy-2-oxo-ethanimidoyl chloride remaining, water (200 mL) was added to the reaction mixture, and the layers were separated. The organic layer was washed with water (300 mL) and concentrated under reduced pressure. Toluene was added to the resulting residue, and the mixture was concentrated under reduced pressure to provide the title compound as an oil (144g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349870B2
Source datasetuspto-grants-2013_01
ORD IDord-74561858295a455ab3d0fd9486582400
Source noteuspto-grants-2013_01