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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227828Erstellt: 25. Oktober 2026

4-Aminophenol → 4-(3-Bromopyridin-2-yloxy)benzenamine

https://huagongshe.com/reaction/227828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminophenolHCID 403—
EduktDimethyl SulfoxideHCID 679—
EduktCesium carbonateHCID 10796—
Edukt3-Bromo-2-chloropyridineHCID 693324—
LösungsmittelWaterHCID 962—
Produkt4-(3-Bromopyridin-2-yloxy)benzenamineHCID 57756256—

Reaktionsschritte

3-Bromo-2-chloropyridine (10.3 g, 53.4 mmol), 4-aminophenol (7.00 g, 64.1 mmol), cesium carbonate (34.8 g, 107 mmol), and DMSO (53 ml, 53.4 mmol) were added into a pressure tube. The tube was capped and placed in a preheated oil bath at 130° C. After 16 h, the reaction mixture was stirred and cooled in ice-water. Water was added slowly to the mixture and the product precipitated out as a gray solid. The solids were washed with water, dried under vacuum at RT to afford 4-(3-bromopyridin-2-yloxy)benzenamine. MS Calcd for C11H9BrN2O: [M]+=264. Found [M+H]+=265.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560551B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-0e85f67198c54cf087454c85c3602191
Quellennotizuspto-grants-2009_07