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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943513생성일: 2026년 10월 23일

Sodium Carbonate → 2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene

https://huagongshe.com/ko/reaction/1943513

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Bromo-5-methylthiopheneHCID 69831—
반응물4'-Ethyl-3-fluorobiphenyl-4-boronic acidHCID 53402575—
촉매HCID 178418397HCID 178418397—
용매Toluene ethanolHCID 21863594—
생성물2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiopheneHCID 58160695—

반응 단계

A mixture of 5.0 g (28.2 mmol) of 2-bromo-5-methylthiophene, 7.70 g (28.3 mmol) of 4′-ethyl-3-fluoro-4-biphenylboronic acid, 1.70 g (1.47 mmol) of tetrakis(triphenylphosphine)palladium(0) and 30 ml of 2 N sodium carbonate solution in 90 ml of toluene/ethanol (1:2) is refluxed for 3 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted a number of times with toluene. The combined organic phases are washed with water and sat. sodium chloride solution. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=97:3). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(4′-ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene as a colourless solid (m.p. 102° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394293B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-05f7bf8fa6664e07a70360f0b33c850a
출처 메모uspto-grants-2013_03