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HRID 751351Erstellt: 25. Oktober 2026

Phosphorus oxychloride → 2-(2-Chloropyridin-3-yl)acetonitrile

https://huagongshe.com/reaction/751351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
Edukt3-(Cyanomethyl)pyridin-1-ium-1-olateHCID 243167—
Produkt2-(2-Chloropyridin-3-yl)acetonitrileHCID 1473954342,9%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

(1-oxypyridin-3-yl)acetonitrile (7.5 g, 35.9 mmol) is carefully added to vigorously stirred phosphorous oxychloride (100 mL). The mixture is slowly heated to 80° C. (in 5° C. increments) over 1.5 hr. (CAUTION. If heating is too quick, violent decomposition occurs at ca 70° C.) All the solids dissolved. The reaction is heated at reflux for 3 hr. The excess phosphorous oxychloride is removed and the residue is cautiously treated with cold water. Saturated sodium bicarbonate is added to make the mixture basic, then it is extracted with ethyl acetate (3×). The combined extract is washed with brine, dried, filtered and concentrated. The residue is purified by chromatography eluting with pentane-10 to 100% ether. The second compound off the column is the desired (2-chloropyridin-3-yl)acetonitrile (2.35 g, 42.9% yield) a light brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07405300B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-a60c00aa524246eb92f144e60a468ac9
Quellennotizuspto-grants-2008_07