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HRID 493095作成日:2026年10月25日

Benzofuran → 3-Bromo-1-benzofuran

https://huagongshe.com/reaction/493095

反応式

関与物質

役割名称HCID仕込み量
反応物BenzofuranHCID 9223—
反応物BromineHCID 24408—
反応物2,3-Dibromo-2,3-dihydrobenzofuranHCID 12394037—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物3-Bromo-1-benzofuranHCID 64058990.2%

反応条件

温度0 °C

反応手順

Bromine (13.1 mL, 250 mmol) dissolved in chloroform (50 mL) is added dropwise to a solution of benzo[b]furan (25 g, 210 mmol) in chloroform (200 mL) at −10° C. over 20 minutes. The mixture is then stirred at 0° C. for 1 hour and the volatiles are evaporated. The residue is stirred with ethanol (50 mL) and then filtered. The solid material is washed with diethyl ether (100 mL) on the filter. This furnishes 23.0 g (39%) of 2,3-dibromo-2,3-dihydro-benzo[b]furan as white crystalline material. Potassium hydroxide pellets (9.3 g, 165 mmol) are dissolved in ethanol (40 mL) and cooled to 0° C. 2,3-Dibromo-2,3-dihydro-benzo[b]furan (23.0 g, 82.7 mmol) dissolved in ethanol (90 mL) is added dropwise hereto at a constant temperature of 0° C. After complete addition the mixture is heated to reflux for 2 hours. The mixture is concentrated in vacuo and water (100 mL) is added. The aqueous layer is extracted with ethyl acetate (3×100 mL). The combined organic fractions are washed with brine (100 mL), dried (MgSO4) and concentrated to furnish 14.7g (90%) of the wanted product as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534791B2
出典データセットuspto-grants-2009_05
ORD IDord-b013d651b6574729a4f272e502124691
出典メモuspto-grants-2009_05