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HRID 1901313作成日:2026年10月26日

Hydrochloric Acid → 5-Bromo-7-methoxy-2-benzofurancarboxylic acid

https://huagongshe.com/reaction/1901313

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物BromineHCID 24408—
反応物1-(5-Bromo-7-Methoxy-1-Benzofuran-2-Yl)Ethan-1-OneHCID 1491366—
溶媒1,4-DioxaneHCID 31275—
生成物5-Bromo-7-methoxy-2-benzofurancarboxylic acidHCID 3358971—

反応条件

温度60 °C

反応手順

To 107.6 ml of 5N sodium hydroxide aqueous solution was added dropwise 26.8 g of bromine at a temperature of -5° C. or below. To this was further added dropwise and slowly a 100 ml dioxane solution containing 15.0 g of 2-acetyl-5-bromo-7-methoxybenzofuran obtained in the above step a). After completion of the dropwise addition, the temperature of the resulting reaction solution was increased gradually to 60° C. and then stirred for 30 minutes. After cooling, the resulting reaction solution was adjusted to pH 2 with concentrated hydrochloric acid and then extracted with ethyl acetate. The resulting organic layer was concentrated to dryness, and crystals thus precipitated were collected by filtration to obtain 5-bromo-7-methoxy-2-benzofurancarboxylic acid. The thus obtained crystals were suspended in 200 ml of ethanol, and 10 ml of thionyl chloride was added dropwise to the suspension with stirring at room temperature. The resulting reaction solution was refluxed under heating for 2 hours. After cooling, the thus treated reaction solution was neutralized with saturated sodium bicarbonate aqueous solution, and then mixed with water to collect precipitated crystals by filtration. The crystals thus collected were purified by silica gel column chromatography using chloroform as an eluant to obtain 11.33 g of ethyl 5-bromo-7-methoxy-2-benzofurancarboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576343
出典データセットuspto-grants-1996_11
ORD IDord-ed2b5fda01cb4d32a2b38a1e895c1dc9
出典メモuspto-grants-1996_11