HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264530Generated: October 29, 2026
Triethylamine → 5-Chloro-3-(3,5-difluorophenyl)isoxazole
https://huagongshe.com/reaction/1264530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ethyl 3-(3,5-difluorophenyl)-3-oxopropanoate | HCID 13550003 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Chloro-3-(3,5-difluorophenyl)isoxazole | HCID 18612664 | 35% |
Reaction Steps
A mixture of ethyl 3,5-difluorobenzoylacetate (1.87 g, 8.19 mmol) and hydroxylamine hydrochloride (626 mg, 9.01 mmol) in acetic acid (24 ml) is stirred at reflux for 1 hr. The crude reaction mixture is concentrated in vacuo and azeotroped with toluene twice. The crude material is suspended in phosphorus oxychloride (37 ml) and triethyl amine (2.37 ml, 17.1 mmol) is added slowly. The reaction mixture is stirred at reflux for 2 days, concentrated in vacuo and azeothroped with toluene 3 times. The residue is dissolved in dichloromethane and passed on a plug of silica gel (elution with dichloromethane. After concentration in vacuo, the crude material is purified by flash chromatography (silica gel, dry loading, 5% diethyl ether in hexane) to give 3-(3,5-difluorophenyl)-5-chloroisoxazole (600 mg, 35%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544982B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-990ef87052cc4b5ba17e16574745f767 |
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| Source note | uspto-grants-2003_04 |
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