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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17168Erstellt: 25. Oktober 2026

5-Bromosalicylaldehyde → 5-Bromo-1,2-benzoxazole

https://huagongshe.com/reaction/17168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-BromosalicylaldehydeHCID 72863—
Edukthydroxylamine-O-sulfonic acidHCID 76284—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Bromo-1,2-benzoxazoleHCID 12003029—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 5-bromo-2-hydroxy-benzaldehyde (2.0 g, 10 mmol) in ethanol (10 mL) at room temperature was treated with hydroxylamine-O-sulfonic acid (1.69 g, 15 mmol), stirred for 20 minutes, diluted with dichloromethane (50 mL), cooled to 0° C. and treated with a solution of sodium bicarbonate (3 g) in water (25 mL). The solution was stirred at 0° C. for 30 minutes. The organic layer was removed and the aqueous layer was extracted with dichloromethane. The aqueous layer was treated with additional dichloromethane (50 mL) and stirring was continued for one hour. The layers were separated and the aqueous layer was extracted with dicloromethane. The combined organic layers were washed with brine, dried (MgSO4) and concentrated. The concentrate was recrystallized from ethanol to give 970 mg (49%) yield of the desired product. MS (ESI(−)) m/e 195.9, 197.9 (M−H)−

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737160B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d2a564846363457bbd5a6780f7989129
Quellennotizuspto-grants-2010_06