Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43583Generated: October 26, 2026

Cesium carbonate → Ethyl 5-ethyl-2-(4-nitrophenyl)-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/43583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-Iodo-4-nitrobenzeneHCID 12495—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant4-Oxazolecarboxylic acid, 5-ethyl-, ethyl esterHCID 12214102—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 5-ethyl-2-(4-nitrophenyl)-1,3-oxazole-4-carboxylateHCID 6840611737.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Dioxane (30 mL) was added to ethyl 5-ethyl-1,3-oxazole-4-carboxylate (described in Armarego, Wilfred L. F.; Taguchi, Hiroyasu; Cotton, Richard G. H.; Battiston, Sandra; Leong, Lillian; Eur. J. Med. Chem. Chim. Ther.; 22; 1987; 283-292, 1.69 g, 10 mmol), 1-iodo-4-nitrobenzene (2.74 g, 11 mmol), palladium acetate (179.6 mg, 0.8 mmol), tris(2-methylphenyl)phosphine (0.49 g, 1.6 mmol) and cesium carbonate (3.25 g, 10 mmol), and the mixture was stirred at 100° C. for 13 hours. Water was added, followed by extraction with ethyl acetate and washing with brine. This was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=5/1, 3/1, 2/1) to obtain 1.08 g of the title compound as a colorless solid (37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-90ceebe8cc994cf6baf0a2a04633192b
Source noteuspto-grants-2013_09