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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259575Erstellt: 25. Oktober 2026

Acetone → 2-[3,5-Di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine

https://huagongshe.com/reaction/259575

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktTriphenylphosphineHCID 11776—
EduktPhosphoniumHCID 5460504—
Edukt2-[3,5-Bis(bromomethyl)phenyl][1,3]oxazolo[4,5-b]pyridineHCID 22754828—
EduktLithium ethoxideHCID 23661847—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-[3,5-Di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridineHCID 22754778—

Reaktionsschritte

A mixture of 5 mmoles of the product from Step A and 11.0 mmoles of triphenylphosphine in 15 ml. of dimethylformamide is stirred and refluxed under nitrogen for 3 hours. The mixture is cooled and the phosphonium salt is collected on a filter. A mixture of 4 mmoles of the phosphonium salt, 100 ml. of ethanol, 1 ml. of acetone and 40 ml. of 0.3 N ethanolic lithium ethoxide is stirred at room temperature under nitrogen for 2 hours. Water (100 ml.) is added and the mixture is cooled in an ice-bath. The precipitate is collected and purified by chromatography on silica gel using 2% methanol in chloroform as the eluant to give 2-[3,5-di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04038396
Quelldatensatzuspto-grants-1977_07
ORD IDord-362677798c424949b59f28cd52e55270
Quellennotizuspto-grants-1977_07