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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78147생성일: 2026년 10월 24일

Dimethylformamide → 2-(4-Bromo-benzyloxy)-3-fluoro-pyridine

https://huagongshe.com/ko/reaction/78147

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물4-Bromobenzyl alcoholHCID 70119—
반응물2-Chloro-3-fluoropyridineHCID 2782791—
용매WaterHCID 962—
생성물2-(4-Bromo-benzyloxy)-3-fluoro-pyridineHCID 5925523598%

반응 단계

To an N,N-dimethylformamide (15 mL) solution of (4-bromo-phenyl)-methanol (1.56 g, 8.34 mmol) was added sodium hydride (401 mg, 8.35 mmol, 50% in oil), which was stirred for 5 minutes at room temperature. Then, an N,N-dimethylformamide (5 mL) solution of 2-chloro-3-fluoropyridine (967 mg, 7.35 mmol) was added to this mixture, which was stirred for 1 hour and 10 minutes at room temperature. Water was to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (heptane: ethyl acetate=2:1) to obtain the title compound (2.03 g, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-461f222fd091484488f6bd2d97d92091
출처 메모uspto-grants-2014_09