HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064810Generated: October 26, 2026
2-Bromoethyl ethyl ether → HCID 22272806, compound
https://huagongshe.com/reaction/1064810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethyl ethyl ether | HCID 61141 | — |
| Reactant | 2-[4-[2-(benzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxyphenyl)acetamide | HCID 22272616 | — |
| Catalyst | Potassium Fluoride | HCID 522689 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22272806 | HCID 22272806 | 70% |
Reaction Steps
2-Bromoethyl ethyl ether (2 ml) and potassium fluoride catalyst carried on alumina (40 wt %, 225 mg, 1.51 mmol) were added to a solution of 2-[4-[2-(benzoxazol-2ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxyphenyl)acetamide (150 mg, 0.30 mmol) in acetonitrile (3 ml) followed by stirring for 41 hours. The catalyst was filtered off and the filtrate was diluted with water and extracted with ethyl acetate. The organic layer was washed with a sodium chloride solution and dried over anhydrous sodium sulfate and the solvent was evaporated therefrom. The residue was purified by a preparative thin layer chromatography (developing solvent, chloroform:ammonia-saturated methanol=20:1) and the resulting crude crystals were recrystallized from ethyl acetate-hexane to provide 120 mg (yield 70%) of the desired compound as colorless powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969711B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-a97242acab8944488b23ce99ae3e3ffe |
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| Source note | uspto-grants-2005_11 |
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