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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064942Generated: October 30, 2026

Nitrogen → 5-Methylsulfanylfuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2064942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 5-nitro-2-furoateHCID 70341—
ReactantSodium methanethiolateHCID 4378561—
SolventDimethyl SulfoxideHCID 679—
Product5-Methylsulfanylfuran-2-carboxylic acid ethyl esterHCID 60007000—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of commercially available 5-nitro-furan-2-carboxylic acid ethyl ester (5.00 g, 27.01 mmol) in DMSO (34.5 mL) was treated at rt with sodium methanethiolate (2.05 g 27.82 mmol). The mixture was then stirred at 100° C. overnight, cooled down to rt and treated with sat. aq. NH4Cl (250 mL). The aqueous layer was extracted with EA (3×100 mL). The combined org. extracts were washed with sat. aq. NaHCO3 (100 mL) and brine (100 mL), dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (70:30 hept-EA) gave the title compound. TLC: rf (70:30 hept-EA)=0.52. LC-MS-conditions 02: tR=0.96 min; [M+AcCN+H]+=228.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-388880270fc4471c9980812d4e7fe42b
Source noteuspto-grants-2012_10