HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 517346Erstellt: 25. Oktober 2026
Acetic Acid → 4-Ethoxycarbonylfuran-2-carboxylic acid
https://huagongshe.com/reaction/517346
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Ethyl 3-furoate | HCID 69201 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Ethoxycarbonylfuran-2-carboxylic acid | HCID 53429231 | — |
Reaktionsschritte
3-Furancarboxylic acid ethyl ester (1.4 g, 10.0 mmol) was dissolved in acetic acid (10 mL), bromine (1.6 g, 10.0 mmol) was added, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20). The obtained crude fraction was dissolved in N,N-dimethylformamide (15 mL), palladium acetate (0.18 g, 0.78 mmol), triphenylphosphine (0.41 g, 1.55 mmol), triethylamine (2.2 mL, 15.5 mmol), and water (0.7 mL, 38.8 mmol) were added, and the mixture was stirred at 80° C. overnight under a carbon monoxide atmosphere. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by high performance liquid chromatography to give the title compound (0.47 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09115107B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-c374a461fb674ca48a3a55051d3c3d7a |
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| Quellennotiz | uspto-grants-2015_08 |
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