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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916438Generated: November 2, 2026

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

https://huagongshe.com/reaction/1916438

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

A 1000-mL round bottom flask equipped with a mechanical stirrer, thermometer and addition funnel was charged with 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 a solution of potassium bicarbonate (70 g, 0.70 mol) in water (350 mL) was added dropwise over 1 h while maintaining the reaction 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. The layers were separated, and the organic layer was washed with water (300 mL) and concentrated under reduced pressure. Toluene was added to the resulting residu, and the mixture was again concentrated under reduced pressure to provide the title compound as an oil (144 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618137B2
Source datasetuspto-grants-2013_12
ORD IDord-72fa758374f64d6dbecedc80bf3c82f3
Source noteuspto-grants-2013_12