HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053384Generated: October 26, 2026
2,6-Dichlorobenzaldchloroxime → 2,2-dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide
https://huagongshe.com/reaction/2053384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzaldchloroxime | HCID 2800164 | — |
| Reactant | 2,2-Dichloro-N-(4-ethynylphenyl)Acetamide | HCID 21100338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2,2-dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07326790B2 |
|---|
| Source dataset | uspto-grants-2008_02 |
|---|
| ORD ID | ord-3bbe3440a869427abfbc58814e52f4a4 |
|---|
| Source note | uspto-grants-2008_02 |
|---|