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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23321생성일: 2026년 10월 23일

2,2,3,3-Tetrafluoro-1-propanol → 2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxy-6-(2,2,3,3-tetrafluoropropyloxy)pyridine

https://huagongshe.com/ko/reaction/23321

반응식

참여 물질

역할이름HCID투입량
반응물2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
반응물Sodium hydrideHCID 24758—
반응물2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridineHCID 22572630—
용매SulfolaneHCID 31347—
용매Ethyl acetate pentaneHCID 22335286—
생성물2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxy-6-(2,2,3,3-tetrafluoropropyloxy)pyridineHCID 2257264299.2%

반응 조건

온도110 °C

반응 단계

To a mixture of 2,2,3,3-tetrafluoropropan-1-ol (0.29 g, 2.2 mmol) in dry sulfolane (2 ml) is added NaH (60% in oil, 0.09 g, 2.2 mmol) and 2,6-bis-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridine (0.8 g, 1.8 mmol). After stirring at 110° C. for 3.7 h the mixture is cooled to ambient temperature. The resulting mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed 10 times with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 9/1 v/v) yields the title compound (0.72 g, 57% yield) of m.p. 73-74° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852673B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-facc9139d28f472d8d74f9b9d1df1032
출처 메모uspto-grants-2005_02