HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064850Generated: November 2, 2026
2-Bromoethyl ethyl ether → HCID 22272766, compound
https://huagongshe.com/reaction/1064850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethyl ethyl ether | HCID 61141 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 22272818 | HCID 22272818 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22272766 | HCID 22272766 | 78% |
Reaction Steps
To a solution of this acetamide (500 mg, 1.32 mmol) solution in DMF (12 ml) were added 2-bromoethyl ethyl ether (7 ml) and potassium fluoride 40 wt. % on alumina (40 wt. %, 1.96 g, 13.2 mmol), and the mixture was stirred at room temperature for 5 days. After the catalyst was filtered off, the filtrate was diluted with water and extracted with ethylacetate. The organic layer was washed with a saturated sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was evaporated therefrom. The resulting residue was purified by a silica gel column chromatography (developing solvent; chloroform:methanol=30:1) to provide 448 mg (yield 78%) of N-[2,6-diisopropyl-4-(2-ethoxyethyloxy)phenyl]-2-[4-(3-hydroxypropyl)piperazin-1-yl]acetamide 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-fd7bd103aad048e698887940a7b1fee2 |
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| Source note | uspto-grants-2005_11 |
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