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HRID 361884생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/361884

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물BromineHCID 24408—
반응물1-(5-Bromo-7-Methoxy-1-Benzofuran-2-Yl)Ethan-1-OneHCID 1491366—
용매1,4-DioxaneHCID 31275—
생성물5-Bromo-7-methoxy-2-benzofurancarboxylic acidHCID 3358971—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05866577
출처 데이터셋uspto-grants-1999_02
ORD IDord-1938b36fea4b4363b87cff91f7082adb
출처 메모uspto-grants-1999_02