HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342940Generated: October 30, 2026
Hydroxyamine hydrochloride → 4-(2-Nitro-4-trifluoromethylbenzoyl)-5-methylisoxazole
https://huagongshe.com/reaction/342940
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2-Ethoxymethylene-1-(2-nitro-4-trifluoromethylphenyl)butan-1,3-dione | HCID 53751742 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Nitro-4-trifluoromethylbenzoyl)-5-methylisoxazole | HCID 53848295 | 37.5% |
Reaction Steps
A mixture of crude 2-ethoxymethylene-1-(2-nitro-4-trifluoromethylphenyl)butan-1,3-dione (13.25 g) and hydroxylamine hydrochloride (3.7 g) in ethanol (80 ml) was stirred for 5 hours. The solution was evaporated almost to dryness and the resultant solution was diluted with ethyl acetate (100 ml). The solution was washed with water (3×40 ml), dried (anhydrous sodium sulphate) and filtered. The filtrate was evaporated to dryness. The residue was triturated with a mixture of ether and petroleum spirit (bp 60°-80° C.) (1:1) and the resultant buff solid was filtered off. The solid was dissolved in dichloromethane (100 ml) and filtered through silica. The silica was washed with dichloromethane (100 ml) and the combined filtrates were evaporated to dryness to give 4-(2-nitro-4-trifluoromethylbenzoyl)-5-methylisoxazole (Compound 1, 4.5 g) as an off-white solid mp 85°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859283 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-bf75a48157a34bf79b499d24507dcff5 |
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| Source note | uspto-grants-1999_01 |
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