HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17883Erstellt: 23. Oktober 2026
Acetic Acid → Ethyl 3-[3-(benzyloxy)phenyl]-3-oxopropanoate
https://huagongshe.com/de/reaction/17883
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Diethyl Carbonate | HCID 7766 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-(3-(Phenylmethoxy)phenyl)ethan-1-one | HCID 98689 | — |
| Produkt | Ethyl 3-[3-(benzyloxy)phenyl]-3-oxopropanoate | HCID 10334847 | 84% |
Reaktionsschritte
1-(3-Benzyloxyphenyl)ethanone (218 g, 966.10 mmol) was dissolved in diethyl carbonate and sodium hydride (60% oil) (46.37 g, 1.15 mmol) was slowly added thereto at 0° C., and then stirred for 3 hours at 60° C. After the reaction was completed, ice water and acetic acid were added to the reaction mixture, extracted with ethyl acetate/saturated sodium chloride, the organic layer was separated, and dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:10) to obtain 3-(3-benzyloxyphenyl)-3-oxopropionate ethyl ester (184.68 g, yield 84%) in an oil state.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741323B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-444829afa1d64032803c8a8149fb905d |
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| Quellennotiz | uspto-grants-2010_06 |
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