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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080056Generated: November 1, 2026

Ethyl Acetate → HCID 23130511, compound

https://huagongshe.com/reaction/2080056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromophenolHCID 11563—
Reactant5-Nitrothiophene-2-carbonitrileHCID 519294—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 23130511HCID 2313051162%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-nitrothiophene-2-carbonitrile (1.79 g, 11.6 mmol) and 3-bromophenol (2.00 g, 11.6 mmol) in dimethylsulfoxide (22 mL) was added potassium carbonate (1.76 g, 12.8 mmol), and the solution was stirred at 70° C. for 3 hours. The reaction solution was allowed to room temperature, ethyl acetate and water were added for partitioning, the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1), and 5-(3-bromophenoxy)-thiophene-2-carbonitrile (2.00 g, 62%) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-656bb6ffcca0468b89bdbee05bdd6257
Source noteuspto-grants-2011_04