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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15052Erstellt: 23. Oktober 2026

Ethanol → 5-Chloro-2-ethenylpyridine

https://huagongshe.com/de/reaction/15052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
Edukt2,5-DichloropyridineHCID 27685—
EduktPotassium vinyltrifluoroborateHCID 23679353—
KatalysatorHCID 178478230HCID 178478230—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Chloro-2-ethenylpyridineHCID 1554762669%

Reaktionsschritte

A mixture of 2,5-dichloropyridine (10.0 g), potassium vinyltrifluoroborate (10.86 g), dichloromethane complex (2.5 g) of dichloro-1,1′-bis(diphenylphosphino)-ferrocene palladium (II), triethylamine (14.13 mL) and ethanol (150 mL) was stirred overnight under reflux. After cooling the system to room temperature, ethyl acetate was added, followed by washing with saturated aqueous sodium hydrogencarbonate solution and saturated brine and drying over anhydrous sodium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was distilled under reduced pressure (63° C., 8 mmHg) to provide the title compound (6.50 g, 69%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732456B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9ed94748395b45b697f76c4f2d4a5178
Quellennotizuspto-grants-2010_06