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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1180258생성일: 2026년 10월 27일

1,3-Dibromo-5-fluorobenzene → 3'-Bromo-4,5'-difluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1180258

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dibromo-5-fluorobenzeneHCID 137003—
반응물5-Fluoro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 22180790—
용매1,2-DimethoxyethaneHCID 8071—
생성물3'-Bromo-4,5'-difluorobiphenyl-2-carbonitrileHCID 179648419.4%

반응 조건

온도65 °C

반응 단계

5-Fluoro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzonitrile (0.99 g, 4.0 mmol) and 1,3-dibromo-5-fluorobenzene (1.52 g, 6.0 mmol) were suspended in 1,2-dimethoxyethane (8 ml) and 2N sodium carbonate solution (4 ml) and degassed for 30 min before addition of tetrakis(triphenylphosphine)palladium(0). On complete addition the mixture was heated at 65° C. for 20 h. The mixture was partitioned between ethyl acetate (100 ml) and water (50 ml), the organic layer separated and washed with brine (50 ml), dried over anhydrous sodium sulphate, filtered and evaporated onto silica. The product was purified by flash column chromatography on silica, eluting with isohexane on a gradient of diethyl ether (5-100%). Combination of the desired fractions and evaporation gave 3′-bromo-4,5′-difluorobiphenyl-2-carbonitrile (110 mg, 9%) as a white solid: δH (500 Mfz, CDCl3) 7.53-7.55 (1H, m), 7.67 (1H, s), 7.69-7.76 (3H, m), 8.03 (1H, dd, J 9 and 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07279580B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-e27e468424f041a391795dfdd250d5e1
출처 메모uspto-grants-2007_10