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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493095생성일: 2026년 10월 24일

Benzofuran → 3-Bromo-1-benzofuran

https://huagongshe.com/ko/reaction/493095

반응식

참여 물질

역할이름HCID투입량
반응물BenzofuranHCID 9223—
반응물BromineHCID 24408—
반응물2,3-Dibromo-2,3-dihydrobenzofuranHCID 12394037—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물3-Bromo-1-benzofuranHCID 64058990.2%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534791B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-b013d651b6574729a4f272e502124691
출처 메모uspto-grants-2009_05