HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860413Erstellt: 24. Oktober 2026
Hydrochloric Acid → Ethyl 7-(4-fluorobenzoyl)-8-oxononanoate
https://huagongshe.com/de/reaction/860413
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Edukt | 1-(4-Fluoro-phenyl)-butane-1,3-dione | HCID 432655 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 7-(4-fluorobenzoyl)-8-oxononanoate | HCID 57444527 | — |
Reaktionsschritte
A mixture of 1-(4-fluorophenyl)butane-1,3-dione (1.0 g), potassium carbonate (3.84 g), and tetrabutylammonium bromide (90 mg) in toluene (20 ml) was refluxed for 3 hours, then ethyl 6-bromohexanoate (1.18 ml) was added. After stirring at 100° C. for 3 hours, the mixture was partitoned between ethyl acetate and 0.5N hydrochloric acid. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 7-(4-fluorobenzoyl)-8-oxononanoate (983 mg) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07153854B2 |
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| Quelldatensatz | uspto-grants-2006_12 |
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| ORD ID | ord-1b492a1ead7a4f64b5ca605ce0ca112b |
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| Quellennotiz | uspto-grants-2006_12 |
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