Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390663Generated: October 27, 2026

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

https://huagongshe.com/reaction/2390663

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 dichloromethane. 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 numberUS08273736B2
Source datasetuspto-grants-2012_09
ORD IDord-4ff4238b74784edbbe8a41715325df33
Source noteuspto-grants-2012_09