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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108352Generated: October 29, 2026

2,6-Dichlorobenzaldchloroxime → HCID 57443467, compound

https://huagongshe.com/reaction/2108352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzaldchloroximeHCID 2800164—
Reactant4-EthynylbenzonitrileHCID 4547245—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 57443467HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514434B2
Source datasetuspto-grants-2009_04
ORD IDord-d2862370b5f24592b9718df080356ab8
Source noteuspto-grants-2009_04