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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053313Generated: October 26, 2026

Potassium Carbonate → Ethyl 3-(4-sulfamoylphenyl)furan-2-carboxylate

https://huagongshe.com/reaction/1053313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Aminosulphonyl)benzeneboronic acidHCID 22391977—
ReactantEthyl 3-bromofuran-2-carboxylateHCID 22456149—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductEthyl 3-(4-sulfamoylphenyl)furan-2-carboxylateHCID 6828577255.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

(4-sulfamoylphenyl)boronic acid (1.76. gm, 8.77 mmol) and Potassium carbonate (2.52 gm, 18.26 mmol) were added to a stirred suspension of ethyl 3-bromofuran-2-carboxylate (Prepared according to the procedure reported in the literature EP1489077A1, 2004, 1.6 gm, 7.30 mmol) in a mixture of 80 ml of ethanol and 20 ml of toluene (80 ml:20 ml) under nitrogen atmosphere at room temperature (25° C.) in a tube. A nitrogen gas was purged to the suspension for 15 minute at room temperature (about 25° C.). To the reaction mixture was then added Tetrakis(triphenyl phosphine)Palladium(0) (0.422 gm, 0.365 mmol) at 25° C. and tube was sealed. The reaction mixture was then stirred at 100° C. for 18 hours. The progress of the reaction was monitored by TLC. The reaction mixture was then filtered and washed with ethyl acetate (2×100 ml). The combined organic layer was then concentrated under reduced pressure to obtain a crude product as semi-solid (11.2 gm), which was then purified by column chromatography over silica gel (100-200 mesh) using 50% ethyl acetate in hexanes as an eluent to obtain the title compound (1.2 g, 55.60%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393247B2
Source datasetuspto-grants-2016_07
ORD IDord-58ed8d3ccf42401aa0587868493cd240
Source noteuspto-grants-2016_07