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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695517Generated: November 2, 2026

Potassium Carbonate → Ethyl 2-(3-methanesulphonylphenyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/1695517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromo-1,3-thiazole-4-carboxylateHCID 353965—
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
CatalystHCID 178456358HCID 178456358—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(3-methanesulphonylphenyl)thiazole-4-carboxylateHCID 6727720547.7%

Reaction Steps

Ethyl 2-bromothiazole-4-carboxylate (1 g), 3-(methylsulphonyl)phenyl-boronic acid (1.02 g, 1.2 equivalents) and potassium carbonate (1.76 g) are introduced in dioxane (12.5 ml). (1,3-Diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(II) dichloride (288 mg) is added, and the mixture is stirred under reflux under protective gas for 18 h. Dioxane is then removed in a rotary evaporator, and the residue is taken up in ethyl acetate and water. The organic phase is separated off and the aqueous phase is back-extracted twice with ethyl acetate. The combined organic phases are washed with brine and dried over sodium sulphate and concentrated. Purification by column chromatography on silica gel (ethyl acetate/hexane) results in a white solid (629 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163739B2
Source datasetuspto-grants-2012_04
ORD IDord-75f1eea9453248d1a790e15de0fcd9c2
Source noteuspto-grants-2012_04