HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1440792Erstellt: 25. Oktober 2026
Hydrochloric Acid → Ethyl 5-oxo-2-(2-chlorobenzoyl)laurate
https://huagongshe.com/reaction/1440792
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1-Decen-3-one | HCID 171530 | — |
| Edukt | Ethyl (2-chlorobenzoyl)acetate | HCID 292405 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Ethyl 5-oxo-2-(2-chlorobenzoyl)laurate | HCID 18981976 | 59,1% |
Reaktionsschritte
To a stirred solution of 0.91 g of ethyl 2-chlorobenzoylacetate in 10 cc of ethanol was added 0.27 g of sodium ethoxide at room temperature, and the mixture was stirred at room temperature for 10 minutes. Then, 0.62 g of 3-oxo-1-decene in 10 cc of ethanol was added and the resulting mixture was stirred overnight at room temperature. Water was added to the reaction mixture, and the aqueous layer was acidified with 1N HCl and extracted three times with ethyl acetate. The combined organic layer was washed with a saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was distilled off and the crude product thus obtained was purified by a silica gel column chromatography (eluent: ethyl acetate/hexane =1/9) to obtain 0.90 g of compound I. Yield: 59.1%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05500424 |
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| Quelldatensatz | uspto-grants-1996_03 |
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| ORD ID | ord-56de54e293c949128f37d7aafeb77437 |
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| Quellennotiz | uspto-grants-1996_03 |
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