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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053269Generated: November 1, 2026

Ethanol → HCID 68285874, compound

https://huagongshe.com/reaction/1053269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Aminosulphonyl)benzeneboronic acidHCID 22391977—
ReactantHCID 68285842HCID 68285842—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 68285874HCID 6828587476.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

To the solution of Ethyl 3-bromo-5-(4-chlorophenyl)thiophene-2-carboxylate (compound 33a, 1.45 g, 4.19 mmol) in a mixture of toluene: ethanol (10:40 ml) was added (4-sulfamoylphenyl)boronic acid (0.84 g, 4.19 mmol) and potassium carbonate (1.16 g, 8.39 mmol) at 25° C. Nitrogen gas was bubbled through the reaction mixture for 15 minutes. To the reaction mixture was then added tetrakis(triphenylphosphine)palladium(0) (0.24 g, 0.20 mmol) under nitrogen atmosphere and the reaction mixture was heated at about 95 to about 100° C. for 16 hr under stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and filtered through celite, the celite cake was washed with Ethanol (2×25 ml). The filtrate so obtained was concentrated under reduced pressure to obtain a crude product, 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 (1.35 g, 76.27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393247B2
Source datasetuspto-grants-2016_07
ORD IDord-33036492e17c4f0fb3a6ead88658fe0c
Source noteuspto-grants-2016_07