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HRID 1870Erstellt: 23. Oktober 2026

Iodoethane → 2-Propyl-3,4,5,6-tetrafluoropyridine

https://huagongshe.com/de/reaction/1870

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktHexaneHCID 8058—
EduktLithium diisopropylamideHCID 2724682—
Edukt2,3,4,5-Tetrafluoro-6-methylpyridineHCID 15388342—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-Propyl-3,4,5,6-tetrafluoropyridineHCID 19691283—

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

A 1.5M solution of LDA in hexane (100 mL, 150 mmol) is cooled to -60° C. in an isopropyl alcohol/dry ice bath. To the stirred LDA solution, under nitrogen, is added, dropwise over a 0.5 hours period, a solution of 22.617 g (137 mmol) of 3,4,5,6-tetrafluoro-2-picoline, the product of Step 1, in 80 mL of dry THF. The reaction mixture is stirred for 0.5 hours at -60° C. and then a solution of 10.95 mL (137 mmol) of ethyl iodide in 30 mL of dry THF is added, dropwise over a 20 minute period. After the reaction mixture is stirred at -60° C. for 0.5 hours, the cooling bath is allowed to slowly (1.5 hours) warm to -30° C. The reaction mixture is poured into cold brine and the aqueous mixture is extracted with methylene chloride. The organic extract is dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue is distilled to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726182
Quelldatensatzuspto-grants-1998_03
ORD IDord-487343b7458b49df9d5c356386d96e9c
Quellennotizuspto-grants-1998_03