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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332616Erstellt: 25. Oktober 2026

Hydrochloric Acid → 5-Hydroxymethyl-3-furancarboxylic acid ethyl ester

https://huagongshe.com/reaction/332616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
EduktSodium borohydrideHCID 4311764—
Edukt4-Ethoxycarbonylfuran-2-carboxylic acidHCID 53429231—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Hydroxymethyl-3-furancarboxylic acid ethyl esterHCID 5947873679%

Reaktionsschritte

4-Ethoxycarbonylfuran-2-carboxylic acid (0.47 g, 2.53 mmol) was dissolved in tetrahydrofuran (10 mL), triethylamine (0.53 mL, 3.80 mmol) and ethyl chloroformate (0.29 mL, 3.04 mmol) were added at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered through celite, water (0.23 mL, 12.7 mmol) and sodium borohydride (0.19 g, 5.06 mmol) were added to the filtrate, and the mixture was stirred overnight. 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 silica gel column chromatography (hexane/ethyl acetate=50/50) to give the title compound (0.34 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877805B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-65eda0e008bb4d8eb24d5cbd8b19000b
Quellennotizuspto-grants-2014_11