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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47354Erstellt: 25. Oktober 2026

Potassium Fluoride → 4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehyde

https://huagongshe.com/reaction/47354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium FluorideHCID 522689—
EduktStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Edukt2-Fluoro-4-iodopyridine-3-carbaldehydeHCID 9992328—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(1-Ethoxyvinyl)-2-fluoro-3-pyridinecarbaldehydeHCID 22745018—

Reaktionsschritte

There are mixed in succession 8 g (31.9 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde (described in J.O.C, 1993, 58, pp. 7832), 12.7 g (35.96 mmol) of 1-ethoxyvinyltributyltin and 740 mg of tetrakis(triphenylphosphine)palladium (2% molar) in 280 ml of dioxane. The reaction mixture is heated at reflux until the starting material has disappeared completely. After returning to room temperature a solution of potassium fluoride is added to the reaction mixture. Vigorous stirring is maintained for 10 minutes in order to cause precipitation of the tributyltin fluoride, which is filtered off. The filtrate is plunged into a sodium chloride solution. The aqueous phase is extracted 3 times with dichloromethane and then the organic phases are combined, dried over magnesium sulphate, concentrated and purified by chromatography over a silica column, using a dichloromethane/cyclohexane mixture (95/5) as eluant to yield the expected product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699876B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-b1911e1b043043799444f39d04e81d1e
Quellennotizuspto-grants-2004_03