참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2-Bromo-5-methylthiophene | HCID 69831 | — |
| 반응물 | 4'-Ethyl-3-fluorobiphenyl-4-boronic acid | HCID 53402575 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Toluene ethanol | HCID 21863594 | — |
| 생성물 | 2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-methylthiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08394293B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-05f7bf8fa6664e07a70360f0b33c850a |
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| 출처 메모 | uspto-grants-2013_03 |
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