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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352227Generated: October 26, 2026

2,6-Dichlorobenzaldchloroxime → 2,2-dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide

https://huagongshe.com/reaction/1352227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzaldchloroximeHCID 2800164—
Reactant2,2-Dichloro-N-(4-ethynylphenyl)AcetamideHCID 21100338—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product2,2-dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamideHCID 10341825—

Reaction Steps

2,6-Dichloro-N-hydroxybenzenecarboximidoyl chloride (1.01 g, 4.5 mmol) and 2,2-dichloro-N-(4-ethynylphenyl)acetamide (1.01 g, 4.42 mmol) were dissolved in anhydrous THF (40 mL) and triethylamine (1.0 mL). The mixture was stirred at room temperature for 1 h then heated at reflux for 4 h to generate the 2,6-dichlorophenyl nitrile oxide intermediate, which reacted by a 1,3-dipolar cycloaddition reaction with 2,2-dichloro-N-(4-ethynylphenyl)acetamide. 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 8:2 hexanes-ethyl acetate. The appropriate fractions were combined to give 2,2-dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220745B2
Source datasetuspto-grants-2007_05
ORD IDord-34d11512bd554aa5b36312773eff7fa2
Source noteuspto-grants-2007_05