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HRID 1361899作成日:2026年10月25日

Iodoethane → Ethyl 3-bromofuran-2-carboxylate

https://huagongshe.com/reaction/1361899

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Cesium carbonateHCID 10796—
反応物Sodium BicarbonateHCID 516892—
反応物3-Bromofuran-2-carboxylic acidHCID 605479—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 3-bromofuran-2-carboxylateHCID 2245614954.3%

反応条件

温度80 °C

反応手順

3-Bromofuran-2-carboxylic acid (1.86 g, 9.75 mmol), ethyl iodide (3.1 mL, 38.8 mol) and cesium carbonate (4.80 g, 14.7 mmol) were suspended in acetonitrile (50 mL), followed by stirring at 80° C. for 3 hours. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=9:1) to afford ethyl 3-bromofuran-2-carboxylate (1.16 g, 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07880013B2
出典データセットuspto-grants-2011_02
ORD IDord-d5bfc4c465ad4b3bbd3874a6474ffd1b
出典メモuspto-grants-2011_02