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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 2,6-Difluorostyrene | HCID 2778300 | — |
| Reactant | Ethanimidoyl chloride, 2-(dimethylamino)-N-hydroxy-2-oxo- | HCID 53423335 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 5-(2,6-Difluorophenyl)-N,N-dimethyl-4,5-dihydroisoxazole-3-carboxamide | HCID 66618229 | 94.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618137B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-72fa758374f64d6dbecedc80bf3c82f3 |
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| Source note | uspto-grants-2013_12 |
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