HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437213Generated: November 2, 2026
Diethyl Ether → 2-Fluoro-1-phenylethan-1-one
https://huagongshe.com/reaction/1437213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Fluoro-1-phenylethan-1-one | HCID 9947 | — |
Reaction Steps
A suspension of potassium fluoride (3.091 g) and 18-crown-6-ether (0.341 g) in acetonitrile (25 mL) was stirred at 55° C. for 1 hour. α-Bromoacetophenone (5.12 g) was added to the reaction mixture, followed by stirring for 20 hours. Subsequently, diethyl ether was added to the reaction mixture, and then the insoluble matter that was formed was removed by filtration. Water was added for partitioning the filtrate. The organic layer was sequentially washed with water and saturated brine. Subsequently, the organic layer was dried over sodium sulfate anhydrate, followed by filtration. The solvent was evaporated under reduced pressure, to thereby give the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622471B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-ac3fdffeb2df48fda35063025a4d142e |
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| Source note | uspto-grants-2009_11 |
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