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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75168Generated: October 30, 2026

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

https://huagongshe.com/reaction/75168

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 6661822994.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a 1 L round bottom flask equipped with a mechanical stirrer, thermometer and addition funnel was added 2-(dimethylamino)-N-hydroxy-2-oxoethanimidoyl chloride (94.0 g, 0.62 mol) and 2,6-difluorostyrene (84.0 g, 0.60 mol) in chlorobenzene (275 g). The reaction mixture was cooled to 10° C., and then potassium bicarbonate (70 g, 0.70 mol) in water (350 mL) was added dropwise over 1 h while maintaining the temperature between 10 and 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 (144 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835427B2
Source datasetuspto-grants-2014_09
ORD IDord-2f2a20fbde1a40679f120ebea0a733d7
Source noteuspto-grants-2014_09