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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629441생성일: 2026년 10월 25일

1,2-Dimethoxyethane → methyl 5-(4-(1H-pyrazol-1-yl)benzyl)-3-fluoro-2-hydroxy-4-methylbenzoate

https://huagongshe.com/reaction/629441

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Sodium CarbonateHCID 10340—
반응물1-[4-(chloromethyl)phenyl]-1H-pyrazoleHCID 7130887—
반응물Methyl 3-fluoro-2-hydroxy-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 131735372—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물methyl 5-(4-(1H-pyrazol-1-yl)benzyl)-3-fluoro-2-hydroxy-4-methylbenzoateHCID 11846811083.7%

반응 조건

온도80 °C

반응 단계

Tetrakis(triphenylphosphine)palladium(0) (2.52 g) was added to a mixture of methyl 3-fluoro-2-hydroxy-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (13.5 g), 1-(4-(chloromethyl)phenyl)-1H-pyrazole (8.39 g), sodium carbonate (9.23 g), DME (195 mL) and water (65.0 mL) under argon atmosphere, and the mixture was stirred overnight at 80° C. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with a mixed solvent of diisopropyl ether-ethyl acetate to give a crude product. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol). The obtained crude products are combined, and washed with diisopropyl ether-ethyl acetate to give the title compound (12.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315458B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-5e3edaf7ebf442bfa2eb72343ceb757a
출처 메모uspto-grants-2016_04