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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573112생성일: 2026년 10월 26일

Dimethylformamide → Methyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/573112

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl 2,4-DifluorobenzoateHCID 2782897—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-Chloro-3-fluoro-5-hydroxypyridineHCID 40424737—
용매2-MethyltetrahydrofuranHCID 7301—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoateHCID 86642876—

반응 단계

To a solution of 6-chloro-5-fluoropyridin-3-ol (0.977 g) in 2-methyltetrahydrofuran (12 mL) was added potassium 2-methylpropan-2-olate (1.0M in tetrahydrofuran, 7.28 mL). After stirring for 15 minutes at room temperature, methyl 2,4-difluorobenzoate (1.710 g) was added as a solution in 2-methyltetrahydrofuran (2 mL) followed by N,N-dimethylformamide (2 mL) then the reaction was heated to 75° C. under a nitrogen atmosphere. After stirring overnight the reaction was cooled, diluted with ethyl acetate (100 mL) and washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (GraceResolv 40 g) eluting with a gradient of 2% to 15% ethyl acetate/hexanes gave the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029404B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-83abc5fa911a4bf9b6f6b3b079582642
출처 메모uspto-grants-2015_05