HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1877041Erstellt: 26. Oktober 2026
Hydrochloric Acid → Methyl 5-bromo-2-(ethoxymethyl)furan-3-carboxylate
https://huagongshe.com/reaction/1877041
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate | HCID 15534191 | — |
| Edukt | Ethanol sodium ethoxide | HCID 23706232 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Methyl 5-bromo-2-(ethoxymethyl)furan-3-carboxylate | HCID 68515316 | 70,5% |
Reaktionsschritte
To a solution of methyl 5-bromo-2-(bromomethyl)furan-3-carboxylate (4.5 g) in ethanol (50 mL) was added 20% sodium ethoxide-ethanol solution (7.8 g) at 0° C., and the mixture was stirred at 0° C. for 2 hr and at room temperature overnight. The reaction was poured into water, and the mixture was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (0% ethyl acetate/hexane to 15% ethyl acetate/hexane) to give the title compound (2.8 g, 67%) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08309580B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-e39c62e7d8ed4c7787a016bcd89160a4 |
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| Quellennotiz | uspto-grants-2012_11 |
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