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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691184생성일: 2026년 10월 27일

Dimethylformamide → 2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehyde

https://huagongshe.com/reaction/1691184

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-Fluoro-4-hydroxybenzaldehydeHCID 587246—
반응물2-(Chloromethyl)-5-fluoropyridineHCID 21698059—
용매WaterHCID 962—
생성물2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehydeHCID 5925535642.2%

반응 단계

To an N,N-dimethylformamide (20.0 mL) solution of 2-fluoro-4-hydroxy-benzaldehyde (1.48 g, 10.2 mmol) was added sodium hydride (411 mg, 10.3 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 20 minutes at room temperature. 2-Chloromethyl-5-fluoro-pyridine (1.20 g, 8.56 mmol) described in Manufacturing Example 41-1-2 was then added at room temperature, and stirred for 30 minutes at 80° C. Water was added at room temperature to the reaction solution, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:5-1:2) to obtain the title compound (901 mg, 42.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153662B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-0d757fab43b1406b855cf028e8fc9a1e
출처 메모uspto-grants-2012_04