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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23422생성일: 2026년 10월 23일

4-Fluorophenol → 3-Bromo-5-(4-fluorophenoxy)pyridine

https://huagongshe.com/ko/reaction/23422

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorophenolHCID 9732—
반응물Sodium HydroxideHCID 14798—
반응물Sodium hydrideHCID 24758—
반응물3,5-DibromopyridineHCID 69369—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-Bromo-5-(4-fluorophenoxy)pyridineHCID 2257390821%

반응 단계

Sodium hydride (1.53 g of 80% in mineral oil, 51 mmol) was slowly added to a solution of 4-fluorophenol (5.6 g, 50 mmol) in DMF (100 mL) as it was stirred and cooled (ice water bath) under a nitrogen atmosphere. The resulting mixture was warmed to ambient temperature and stirred for 1 h. 3,5-Dibromopyridine (5.9 g, 25 mmol) was added and the mixture was then heated at 90° C. (bath temperature) for 62 h. The mixture was cooled, diluted with water (150 mL), poured into 5N sodium hydroxide (150 mL), and extracted with diethyl ether (2×150 mL). The combined ether extracts were washed with water, dried (MgSO4), filtered and concentrated by rotary evaporation. The residue was purified by flash chromatography on silica gel, using 5% ethyl acetate:hexane as eluent, to yield 1.4 g (21%) of a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852721B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8aade8a04c6e4434b04d077cde5d80c5
출처 메모uspto-grants-2005_02