HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108352Generated: October 29, 2026
2,6-Dichlorobenzaldchloroxime → HCID 57443467, compound
https://huagongshe.com/reaction/2108352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzaldchloroxime | HCID 2800164 | — |
| Reactant | 4-Ethynylbenzonitrile | HCID 4547245 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 57443467 | HCID 57443467 | — |
Reaction Steps
2,6-Dichloro-N-hydroxybenzenecarboximidoyl chloride (2.67 g, 11.9 mmol) and 4-ethynylbenzonitrile (1.50 g, 11.9 mmol) were dissolved in anhydrous tetrahydrofuran (150 mL) and triethylamine (2.15 mL). The mixture was stirred at room temperature for 1 h then heated at reflux for 6 h to generate the 2,6-dichlorophenyl nitrile oxide intermediate, which reacted by a 1,3-dipolar cycloaddition reaction with 4-ethynylbenzonitrile. The solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate and washed successively with water and brine. The ethyl acetate solution was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting solid was purified by column chromatography on silica gel, eluting with 7:3 hexanes-ethyl acetate. The appropriate fractions were combined to give 3-(2,6-dichlorophenyl)-5-(4-cyanophenyl) isoxazole as a white solid, 0.58 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514434B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-d2862370b5f24592b9718df080356ab8 |
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| Source note | uspto-grants-2009_04 |
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