HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053386Generated: October 30, 2026
Dichloroacetyl chloride → HCID 3007230, compound
https://huagongshe.com/reaction/2053386
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21100343 | HCID 21100343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 3007230 | HCID 3007230 | — |
Reaction Steps
3-(3-Aminophenyl)-5-(2,6-dichlorophenyl)isoxazole (60 mg, 0.2 mmol) was dissolved in anhydrous tetrahydrofuran (10 mL) with triethylamine (33 mL, 0.24 mmol). The mixture was cooled in an ice-bath under nitrogen, then a solution of dichloroacetyl chloride (23 mL, 0.24 mmol) in anhydrous tetrahydrofuran (5 mL) was added dropwise. After the addition was completed the ice-bath was removed and the mixture was stirred at room temperature for 12 h. 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 the title compound as a tan solid, 74 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326790B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-75e71b20ff534386b3298802d2571d43 |
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| Source note | uspto-grants-2008_02 |
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