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HRID 43559作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/43559

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium BicarbonateHCID 516892—
反応物4-Nitrophenylboronic acidHCID 2773552—
反応物Ethyl 2-bromothiazole-5-carboxylateHCID 3614103—
触媒HCID 178418397HCID 178418397—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 2-(4-nitrophenyl)-1,3-thiazole-5-carboxylateHCID 5340366054%

反応条件

温度100 °C

反応手順

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%).

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-140d3066c5b543dbb493723739923163
出典メモuspto-grants-2013_09