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HRID 253984作成日:2026年10月27日

Ethanol → Ethyl alpha-oxofuran-2-acetate

https://huagongshe.com/reaction/253984

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sulfuric AcidHCID 1118—
反応物2-Furylglyoxylic acidHCID 73846—
溶媒ChloroformHCID 6212—
生成物Ethyl alpha-oxofuran-2-acetateHCID 7423086.2%

反応条件

温度65 °C

反応手順

2-(Furan-2-yl)-2-oxoacetic acid (15.0 g, 107 mmol) was dissolved in chloroform (420 mL) and treated with EtOH (165 mmol) and H2SO4 (1 mL). The reaction was heated to 65° C. overnight, at which point LC-MS indicated disappearance of starting material and product formation. The crude reaction was cooled and washed with sat. aq. NaHCO3 (3×100 mL) and brine (100 mL). The organics were concentrated to provide ethyl 2-(furan-2-yl)-2-oxoacetate (15.5 g, 64%) as a brown oil, which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872031B2
出典データセットuspto-grants-2011_01
ORD IDord-eff0ec7040a4433999c4862567c12765
出典メモuspto-grants-2011_01