돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18192생성일: 2026년 10월 24일

Methyl iodide → 7-Bromo-5-fluoro-3-(3-fluoro-benzyl)-2-methanesulfonyl-benzofuran

https://huagongshe.com/ko/reaction/18192

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium SulfiteHCID 24437—
반응물Sodium BicarbonateHCID 516892—
반응물7-Bromo-5-fluoro-3-(3-fluoro-benzyl)-benzofuran-2-sulfonyl chlorideHCID 59344922—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물7-Bromo-5-fluoro-3-(3-fluoro-benzyl)-2-methanesulfonyl-benzofuranHCID 5934493358.2%

반응 단계

7-Bromo-5-fluoro-3-(3-fluoro-benzyl)-benzofuran-2-sulfonyl chloride (0.63 gm, 1.5 mmol) was dissolved in THF (5 ml) and added dropwise to a mixture of sodium sulfite (0.504 gm, 4 mmol) and sodium bicarbonate (0.336 gm, 4 mmol) in water (12 ml). The mixture was refluxed for three hours, cooled to room temperature, and methyl iodide (0.75 ml, 12 mmol) was added. The mixture was heated to 50° C. for two hours then cooled to room temperature and stirred for 16 hours. The mixture was diluted with water and extracted twice with dichloromethane. The solution was dried over magnesium sulfate and purified by preparative thin layer chromatography (1/4, ethyl acetate/hexanes) to give 7-bromo-5-fluoro-3-(3-fluoro-benzyl)-2-methanesulfonyl-benzofuran (0.35 gm, 58% yield), (M+H)+ 402.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741326B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-13b3e87c590b448f8662662dd0cb541e
출처 메모uspto-grants-2010_06