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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridine | HCID 22572630 | — |
| 용매 | Sulfolane | HCID 31347 | — |
| 용매 | Ethyl acetate pentane | HCID 22335286 | — |
| 생성물 | 2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxy-6-(2,2,3,3-tetrafluoropropyloxy)pyridine | HCID 22572642 | 99.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06852673B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-facc9139d28f472d8d74f9b9d1df1032 |
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| 출처 메모 | uspto-grants-2005_02 |
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