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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 646222생성일: 2026년 10월 25일

Sodium Carbonate → 2-Fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridine

https://huagongshe.com/reaction/646222

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Fluoropyridine-3-boronic acidHCID 2783270—
반응물((3-Bromophenyl)ethynyl)trimethylsilaneHCID 3683324—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-Fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridineHCID 6870158792.8%

반응 단계

To a solution of [(3-bromophenyl)ethynyl](trimethyl)silane (2.28 g, 9.0 mmol) in DME (150 mL) is added (2-fluoropyridin-3-yl)boronic acid (1.41 g, 10.0 mmol), tetrakis(triphenylphosphine)palladium (0.52 g, 0.5 mmol) and a solution of sodium carbonate (3.8 g, 36.0 mmol) in H2O (15 mL) at room temperature. After refluxing for 3 h, the reaction mixture is cooled, quenched with saturated sodium carbonate, diluted with EtOAc. The two layers are separated and the aqueous layer is extracted with EtOAc. The combined organic extracts are washed with brine, dried (MgSO4) and concentrated. The crude mixture is purified by chromatography (silica gel, EtOAc/hexane:5/95) to give the 2-fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridine (2.25 g, 91%) as an oil. MS (+) APPI: 270 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705030B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-4b3c217f41ab446ba3f4c2cdb1c4c294
출처 메모uspto-grants-2010_04