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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17168Generated: October 25, 2026

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

https://huagongshe.com/reaction/17168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromosalicylaldehydeHCID 72863—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Bromo-1,2-benzoxazoleHCID 12003029—

Reaction Conditions

Temperature0 °C

Reaction Steps

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)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-d2a564846363457bbd5a6780f7989129
Source noteuspto-grants-2010_06