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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252015생성일: 2026년 10월 24일

Methanol → methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylate

https://huagongshe.com/ko/reaction/252015

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Perfluoro(methyl vinyl ether)HCID 14474—
반응물Potassium HydroxideHCID 14797—
반응물HCID 178469376HCID 178469376—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylateHCID 86632567—

반응 단계

Trifluoromethyl trifluorovinyl ether was blown into a mixture of 1.0 g of ethyl 1-(3-chloro-2-pyridinyl)-3-hydroxy-1H-pyrazole-5-carboxylate, 0.042 g of potassium hydroxide, 10 ml of methanol and 10 ml of dimethyl sulfoxide under ice-cooling. The resulting mixture was stirred at room temperature for 4 days. Water was poured into the reaction mixture, and the mixture was extracted with diethyl ether two times. The organic layers were combined, washed with water and an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography to obtain 1.32 g of methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylate of the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07867949B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-3ef1c3e3bade49ae84d7154df64a69d2
출처 메모uspto-grants-2011_01