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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061829생성일: 2026년 10월 27일

2,6-Dibromopyridine → 2-(6-Bromopyridin-2-yl)benzonitrile

https://huagongshe.com/reaction/1061829

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참여 물질

역할이름HCID투입량
반응물2,6-DibromopyridineHCID 12274—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-(2-Cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 3570229—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물2-(6-Bromopyridin-2-yl)benzonitrileHCID 2218078530.2%

반응 조건

온도80 °C

반응 단계

A mixture of 2,6-dibromopyridine (2.07 g, 8.7 mmol), 2-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)benzonitrile (prepared as described in Tetrahedron (2001), 57(49), 9813-9816, 3.00 g, 13 mmol) and potassium phosphate (3.71 g, 17 mmol) in DMF (40 mL) was degassed with nitrogen. Tetrakis(triphenylphosphine)palladium(0) (303 mg, 0.26 mmol) was added, the mixture was degassed as before, and was then stirred at 80° C. under nitrogen overnight. The mixture was partitioned between water and ethyl acetate, and the resulting aqueous layer was washed with ethyl acetate (2×100 mL). The combined organic layers were washed with water (1×100 mL) and saturated sodium chloride solution (1×100 mL), then were dried over magnesium sulfate and concentrated in vacuo. The residual material was purified by flash chromatography on silica gel, eluting with 50% ethyl acetate in isohexane, affording 2-(6-bromopyridin-2-yl)benzonitrile as a solid (680 mg, 30%). δH (400 MHz, CDCl3) 7.51-7.57 (2H, m), 7.68-7.73 (2H, m), 7.80 (2H, d, J 7.7), 7.91 (1H, dd, J 0.7 and 7.7).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960598B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-5c65db8f744549f98e37bbf5bba44eed
출처 메모uspto-grants-2005_11