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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45570Erstellt: 25. Oktober 2026

Tetrahydrofuran → 2-Cyano-3-fluoropyridine

https://huagongshe.com/reaction/45570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTrifluoroacetic anhydrideHCID 9845—
EduktSodium CarbonateHCID 10340—
Edukt3-Fluoropyridine-2-carboxamideHCID 45079852—
LösungsmittelWaterHCID 962—
Produkt2-Cyano-3-fluoropyridineHCID 7060408—

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

30 g of 3-Fluoropyridine-2-carboxamide (C), 120 mL of THF and 768.5 mL of TEA were taken in a reaction flask and cooled to 0-5° C. To this mixture, 72.2 mL of Trifluoroacetic anhydride (in 30 mL of THF) was added dropwise over a period of 30 minutes keeping the reaction temperature below 5° C. (0° C. to 5° C.) and the RM was stirred for 2 hours 30 minutes at a temperature below 10° C. (5° C. to 10° C.). After completion of the reaction, 150 mL of 20% Na2CO3 solution was added dropwise to the RM while maintaining the temperature below 10° C. (5° C. to 5° C.), followed by addition of 360 mL of purified water. The RM was brought to room temperature (RT) and extracted with dichloromethane (MDC) and the organic layer was washed with 300 mL purified water, 150 mL of 2% dil HCl, followed by purified water and brine. The organic layer was dried over Na2SO4 and distilled under vacuum, resulting in the titled compound as a dark brown viscous oily mass. Crude Yield: 22-24 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541580B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-6b91dab580374ebf8e71fd1c5aba3336
Quellennotizuspto-grants-2013_09