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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78089Erstellt: 23. Oktober 2026

Dimethylformamide → 6-(Pyridin-3-yloxy)-pyridine-3-carbaldehyde

https://huagongshe.com/de/reaction/78089

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt3-HydroxypyridineHCID 7971—
EduktSodium hydrideHCID 24758—
Edukt6-Chloropyridine-3-carbaldehydeHCID 2764053—
LösungsmittelWaterHCID 962—
Produkt6-(Pyridin-3-yloxy)-pyridine-3-carbaldehydeHCID 5925519336%

Reaktionsschritte

To a suspension of sodium hydride (407 mg, 8.48 mmol, 50% in oil) and N,N-dimethylformamide (45 mL) was added an N,N-dimethylformamide (5 mL) solution of 3-hydroxypyridine (806 mg, 8.48 mmol) at 0° C., which was stirred for 30 minutes. An N,N-dimethylformamide (5 mL) solution of 2-chloro-5-formylpyridine (1.0 g, 7.06 mmol) was added to this reaction mixture at the same temperature, which was stirred for 5 hours at 100° C. The reaction mixture was cooled to room temperature, and water was added thereto, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate) to obtain the title compound (505.1 mg, 36%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841327B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-a48fa208865b4d5b8702eea204cd5d0f
Quellennotizuspto-grants-2014_09