HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55548Erstellt: 23. Oktober 2026
2-Fluoroethanol → 3-(2-Fluoroethoxy)-pyrid-2-ylsulfonamide
https://huagongshe.com/de/reaction/55548
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Fluoroethanol | HCID 9737 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Fluoropyridine-2-sulfonamide | HCID 19957930 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(2-Fluoroethoxy)-pyrid-2-ylsulfonamide | HCID 19957936 | — |
Reaktionsschritte
5.76 ml of 2-fluoroethanol are added dropwise, with cooling, to a suspension of 6.54 g of sodium hydride (55.6% NaH in oil) in 120 ml of tetrahydrofuran so that the temperature does not exceed 20° C. When the dropwise addition is complete, the reaction mixture is stirred at room temperature for 15 minutes and then a further solution of 10.56 g of 3-fluoro-pyrid-2-ylsulfonamide in 60 ml of tetrahydrofuran is added dropwise over a period of 10 minutes. The reaction solution is then stirred for 10 minutes at room temperature and for 2 hours at reflux before it is cooled and concentrated. For purification, the oil remaining is chromatographed on a silica gel column using ethyl acetate/hexane 4/1. Evaporation of the eluant yields a light-coloured oil which crystallises spontaneously, yielding 5.88 g of title product which melts at 122°-123° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05625071 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-a73cb883fae1487ca599634bf5ed7e4b |
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| Quellennotiz | uspto-grants-1997_04 |
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