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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 367052Erstellt: 24. Oktober 2026

Acetonitrile → 2-Fluoro-5-nitropyridine

https://huagongshe.com/de/reaction/367052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt2-Chloro-5-nitropyridineHCID 78308—
EduktPotassium FluorideHCID 522689—
KatalysatorTetraphenylphosphonium BromideHCID 2724163—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Fluoro-5-nitropyridineHCID 9526454%

Reaktionsschritte

2-Chloro-5-nitropyridine (100 g, 0.656 mol, Aldrich), potassium fluoride (84.1 g, 1.45 mol, Aldrich), tetraphenylphosphonium bromide (95.3 g, 0.227 mol, Aldrich), and acetonitrile (1.5 L) were combined and heated at reflux until consumption of the 2-chloro-5-nitropyridine was complete. The volume of the mixture was reduced to 750 mL, diluted with 2 L of ether, filtered and concentrated. The resultant residue was triturated with hot hexane, and the combined hexane extracts were concentrated to give of the title compound (48 g, 54%): 1H NMR (CDCl3, 300 MHz) δ 7.15 (dd, J=3, 6 Hz, 1H), 8.64 (m, 1H), 9.15 (d, J=1.6 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06133253
Quelldatensatzuspto-grants-2000_10
ORD IDord-15c08ec3a41c4b66a02a81bb36bd2c99
Quellennotizuspto-grants-2000_10