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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698164Erstellt: 25. Oktober 2026

Methyl 5-bromofuran-2-carboxylate → Methyl 5-(methylsulfonyl)furan-2-carboxylate

https://huagongshe.com/reaction/1698164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 5-bromofuran-2-carboxylateHCID 599633—
EduktSodium methanesulfinateHCID 2733271—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 5-(methylsulfonyl)furan-2-carboxylateHCID 53485860—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

To a solution of 5-bromo-furan-2-carboxylic acid methyl ester (4.7 g, 23 mmol) in DMSO (25 mL) was added the sodium methanesulfinate (5.5 g, 46 mmol) followed by copper (I) iodide (4.4 g, 23 mmol). The mixture was then heated to 110° C. for 2 hours. The reaction was diluted with water (100 mL) and ethyl acetate (100 mL) and filtered through diatomaceous earth. The aqueous layer was separated and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with brine (2×50 mL), dried over sodium sulfate, filtered and concentrated to afford 5-methanesulfonyl-furan-2-carboxylic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163918B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-cabf43c29a0b4b2e9d35550fcb9e02ab
Quellennotizuspto-grants-2012_04