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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233736Erstellt: 25. Oktober 2026

Dimethylformamide → 3-Fluoro-2-pyridinecarboxaldehyde

https://huagongshe.com/reaction/233736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktDabcoHCID 9237—
Edukt3-FluoropyridineHCID 67794—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-Fluoro-2-pyridinecarboxaldehydeHCID 1134401735,2%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

Dry ethyl ether (500 mL), n-BuLi (1.6M in hexane, 62.5 mL, 0.1 mol), and dry 1,4-diazabicyclo[2.2.2]octane (DABCO) (11.56 g, 0.1 mol) were introduced into a 1 L flask under a dry N2 stream at -60° C. and the resulting cloudy solution was stirred for 1 hour at -20° C. The mixture was then cooled to -75° C. and an ethyl ether (50 mL) solution of 3-fluoropyridine (9.81 g, 0.1 mol) was added dropwise and stirring continued for 11/2 hours at -60° C. The mixture was recooled to -75° C., dry N,N-dimethylformamide (8.52 mL, 0.11 mol) dissolved in ethyl ether (50 mL) was added dropwise and the mixture stirred for 2 hours at -75° C. Water (175 mL) was introduced slowly at -10° C., the aqueous layer extracted with ethyl acetate (5×200 mL), and the combined extracts were dried over anhydrous sodium sulfate. Solvent removal produced a dark brown oil which after vacuum distillation and purification by chromatography on silica gel provided 4.4 g (35%) of the titled product as an off-white crystalline solid:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05593993
Quelldatensatzuspto-grants-1997_01
ORD IDord-f9af62d281b04a919bdde32f2d344c26
Quellennotizuspto-grants-1997_01