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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332615Erstellt: 25. Oktober 2026

Acetic Acid → 4-Ethoxycarbonylfuran-2-carboxylic acid

https://huagongshe.com/reaction/332615

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktTriphenylphosphineHCID 11776—
EduktBromineHCID 24408—
EduktEthyl 3-furoateHCID 69201—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Ethoxycarbonylfuran-2-carboxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877805B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-5357d541ba694a70b16c8446760eac70
Quellennotizuspto-grants-2014_11