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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15034생성일: 2026년 10월 23일

Dimethylformamide → 4-benzyloxy-1-{4-[(2-tetrahydropyranyl)oxy]phenyl}-1H-pyridin-2-one

https://huagongshe.com/ko/reaction/15034

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2H-Pyran, tetrahydro-2-(4-iodophenoxy)-HCID 2916803—
반응물4-Benzyloxy-2(1H)-pyridoneHCID 3607724—
용매WaterHCID 962—
생성물4-benzyloxy-1-{4-[(2-tetrahydropyranyl)oxy]phenyl}-1H-pyridin-2-oneHCID 6843067158%

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온도150 °C

반응 단계

A mixture of 4-benzyloxy-1H-pyridin-2-one (7.04 g, 35.0 mmols), 2-[(4-iodophenyl)oxy]tetrahydropyran (13.6 g, 44.8 mmols), cuprous iodide (2.1 g, 11.2 mmols), potassium carbonate (10.3 g, 73.5 mmols) and N,N-dimethylformamide (200 mL) was stirred overnight at 150° C. The reaction liquid was cooled to room temperature, into which water (1.2 L) was poured, and the formed insoluble matter was recovered by filtration. Chloroform (300 mL) was added to the insoluble matter, followed by another filtration. The filtered organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, ethyl acetate was added to the resulting residue. The precipitate was recovered by filtration and dried to provide the title compound (7.6 g, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-eb7b6873e47a44308528e9ab831d00fd
출처 메모uspto-grants-2010_06