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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromosalicylaldehyde | HCID 72863 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-1,2-benzoxazole | HCID 12003029 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737160B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d2a564846363457bbd5a6780f7989129 |
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| Source note | uspto-grants-2010_06 |
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