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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629361생성일: 2026년 10월 26일

Water → methyl 3-chloro-2-hydroxy-5-[4-(1H-pyrazol-1-yl)benzyl]-4-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/629361

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-[4-(chloromethyl)phenyl]-1H-pyrazoleHCID 7130887—
반응물Tripotassium phosphate trihydrateHCID 18407952—
반응물Methyl 3-chloro-2-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoateHCID 131735369—
촉매HCID 178418397HCID 178418397—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물methyl 3-chloro-2-hydroxy-5-[4-(1H-pyrazol-1-yl)benzyl]-4-(trifluoromethyl)benzoateHCID 118468170—
생성물3-chloro-2-hydroxy-5-[4-(1H-pyrazol-1-yl)benzyl]-4-(trifluoromethyl)benzoic acidHCID 118468427—

반응 조건

온도90 °C

반응 단계

To a solution of methyl 3-chloro-2-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate (1.50 g) in 1,4-dioxane (30.0 mL) were added 1-(4-(chloromethyl)phenyl)-1H-pyrazole (0.76 g), tetrakis(triphenylphosphine)palladium(0) (0.23 g) and tripotassium phosphate trihydrate (2.10 g), and the mixture was stirred at 90° C. for 16 hr under nitrogen atmosphere. The reaction mixture was allowed to be cooled to room temperature, water and ethyl acetate were added thereto, and the mixture was partitioned. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by flash silica gel column chromatography (ethyl acetate/petroleum ether) to give methyl 3-chloro-2-hydroxy-5-[4-(1H-pyrazol-1-yl)benzyl]-4-(trifluoromethyl)benzoate (0.12 g) and 3-chloro-2-hydroxy-5-[4-(1H-pyrazol-1-yl)benzyl]-4-(trifluoromethyl)benzoic acid (0.70 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315458B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-32eb98c2ab494121bd3966240aee84c0
출처 메모uspto-grants-2016_04