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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43559Generated: October 26, 2026

Water → Ethyl 2-(4-nitrophenyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/43559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Nitrophenylboronic acidHCID 2773552—
ReactantEthyl 2-bromothiazole-5-carboxylateHCID 3614103—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(4-nitrophenyl)-1,3-thiazole-5-carboxylateHCID 5340366054%

Reaction Conditions

Temperature100 °C

Reaction Steps

Water (5 mL) and 1,4-dioxane (5 mL) were added to 4-nitrophenylboronic acid (667 mg, 4 mmol), ethyl 2-bromo-1,3-thiazole-5-carboxylate (448 μL, 4 mmol), sodium bicarbonate (1.01 g, 12 mmol) and tetrakis(triphenylphosphine)palladium (462 mg, 0.4 mmol), and the mixture was stirred in a nitrogen atmosphere at 100° C. for 1.5 hours. Ethyl acetate was added to the reaction solution, and the organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=10/1, 4/1, 2/1) to obtain 0.6 g of the title compound as a colorless solid (54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-140d3066c5b543dbb493723739923163
Source noteuspto-grants-2013_09