Reaktion #431875
ord-51fd0243d6b04062a1810d51847ac00e
Reaktionsgleichung
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturthe whole is heated
- 2Temperaturunder reflux for 10 hours
- 3TemperaturAfter cooling
- 4Sonstigedecanting
- 5workup.ADDITIONether is added
- 6Filtrationafter filtering
Vorschrift
5 g of 3-(5-methyloxazol-2-yl)-pyridine prepared as indicated in Chimica Therap 4, 437 (1973) is dissolved in 50 cm3 of ethanol, 3 cm3 of iodomethane is added and the whole is heated under reflux for 10 hours. After cooling and decanting, ether is added, and after filtering, 8.68 g of product is obtained. M.p.=147°-148° C., after crystallization from ethanol.