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
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
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835427B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2f2a20fbde1a40679f120ebea0a733d7 |
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| Source note | uspto-grants-2014_09 |
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