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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198134Generated: October 31, 2026

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

https://huagongshe.com/reaction/2198134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-bromofuran-2-carboxylateHCID 599633—
ReactantSodium methanesulfinateHCID 2733271—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-(methylsulfonyl)furan-2-carboxylateHCID 53485860—

Reaction Conditions

Temperature110 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-21509a719ce14c2db2723c8e3cee9a42
Source noteuspto-grants-2012_12