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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272204Generated: November 1, 2026

Sodium Carbonate → HCID 22723451, compound

https://huagongshe.com/reaction/1272204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
SolventEthyl AcetateHCID 8857—
ProductHCID 22723451HCID 2272345170%

Reaction Conditions

Temperature88 °C

Reaction Steps

A 25 ml 1-propanol solution of 2-methoxyphenyl boronic acid (1.2 g, 7.5 mmol) and 5-bromothien-2-ylsulfonamide (1.2 g, 5 mmol) is stirred under N2 at room temperature. Palladium(II) acetate (56 mg, 0.25 mmol), triphenylphosphine (200 mg, 0.75 mmol), 2M aqueous Na2CO3 (3 ml, 6 mmol), and 7 ml H2O are added and the resulting mixture is refluxed (˜88° C.) for 1 hour. The reaction is cooled, diluted with ethyl acetate, washed with brine, and the brine back extracted with ethyl acetate. The extracts are combined, washed with aqueous NaHCO3, brine, dried (Na2SO4), filtered, and the filtrate is concentrated. The residue is purified by chromatography (SiO2, ethyl acetate/hexane gradient) to give 943 mg (70%) of 5-(2-methoxyphenyl)thiophene-2-sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208505B2
Source datasetuspto-grants-2007_04
ORD IDord-8f33dd70aa894ed99e3d9568e1b29e61
Source noteuspto-grants-2007_04