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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 224875Erstellt: 24. Oktober 2026

3-Acetylpyridine → ethyl (2Z)-3-(pyridin-3-yl)but-2-enoate

https://huagongshe.com/de/reaction/224875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-AcetylpyridineHCID 9589—
Edukt(Ethoxycarbonylmethyl)triphenylphosphonium bromideHCID 73731—
EduktSodium ethoxideHCID 2723922—
LösungsmittelEthanolHCID 702—
Produktethyl (2Z)-3-(pyridin-3-yl)but-2-enoateHCID 67402107111,3%

Reaktionsschritte

Ethoxycarbonylmethyltriphenylphosphonium bromide (100 g) in ethanol (500 ml) was added with stirring under nitrogen to a solution of sodium ethoxide (from 4.28 g sodium) in ethanol (100 ml). 3-Acetylpyridine (18.8 g) in ethanol (300 ml) was added dropwise over 0.5 hour. The mixture was allowed to stand for 14 days and was evaporated to dryness. The residue was taken up in water, the pH adjusted to 8.5 and the mixture was extracted with benzene. The extract was dried, evaporated and the residue was distilled at reduced pressure to give ethyl 3-(3-pyridyl)-crotonate (13.39 g) b.p. 78°/0.1 mmHg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04234588
Quelldatensatzuspto-grants-1980_11
ORD IDord-e810e93309c649d99782bfc28a9990d6
Quellennotizuspto-grants-1980_11