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HRID 23321Erstellt: 23. Oktober 2026
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/de/reaction/23321
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2,6-Bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxypyridine | HCID 22572630 | — |
| Lösungsmittel | Sulfolane | HCID 31347 | — |
| Lösungsmittel | Ethyl acetate pentane | HCID 22335286 | — |
| Produkt | 2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methoxy-6-(2,2,3,3-tetrafluoropropyloxy)pyridine | HCID 22572642 | 99,2% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852673B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-facc9139d28f472d8d74f9b9d1df1032 |
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| Quellennotiz | uspto-grants-2005_02 |
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