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HRID 43583作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/43583

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1-Iodo-4-nitrobenzeneHCID 12495—
反応物Tri-o-tolylphosphineHCID 80271—
反応物4-Oxazolecarboxylic acid, 5-ethyl-, ethyl esterHCID 12214102—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 5-ethyl-2-(4-nitrophenyl)-1,3-oxazole-4-carboxylateHCID 6840611737.2%

反応条件

温度100 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536197B2
出典データセットuspto-grants-2013_09
ORD IDord-90ceebe8cc994cf6baf0a2a04633192b
出典メモuspto-grants-2013_09