HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15131Erstellt: 26. Oktober 2026
Acetonitrile → 1,1-Dimethylethyl [5-fluoro-2-(fluoroacetyl)-6-(methyloxy)-3-pyridinyl]carbamate
https://huagongshe.com/reaction/15131
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Selectfluor | HCID 2724933 | — |
| Edukt | 1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate | HCID 86614146 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,1-Dimethylethyl [5-fluoro-2-(fluoroacetyl)-6-(methyloxy)-3-pyridinyl]carbamate | HCID 86614147 | — |
Reaktionsschritte
A mixture of 1,1-dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate (6.72 g, 21.54 mmol), acetonitrile (70 ml), and saturated aqueous sodium bicarbonate solution (15 ml) was treated portionwise over 5 minutes at 0° C. under argon with [1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor™) (8.9 g, 25.05 mmol). After the addition the mixture was stirred at room temperature for 0.5 hour then treated with saturated aqueous sodium bicarbonate solution (50 ml), stirred for 10 minutes, then diluted with water (100 ml) and extracted with ethyl acetate (3×200 ml). The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed eluting with 0-50% dichloromethane in hexane affording the product as a white solid (3.72 g, 57%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732460B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-bafbb154d86e4eac85d553a85bf98cb2 |
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| Quellennotiz | uspto-grants-2010_06 |
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