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HRID 252015作成日:2026年10月25日

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

https://huagongshe.com/reaction/252015

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Perfluoro(methyl vinyl ether)HCID 14474—
反応物Potassium HydroxideHCID 14797—
反応物HCID 178469376HCID 178469376—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物methyl 1-(3-chloro-2-pyridinyl)-3-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]-1H-pyrazole-5-carboxylateHCID 86632567—

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867949B2
出典データセットuspto-grants-2011_01
ORD IDord-3ef1c3e3bade49ae84d7154df64a69d2
出典メモuspto-grants-2011_01