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HRID 17168作成日:2026年10月27日

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

https://huagongshe.com/reaction/17168

反応式

関与物質

役割名称HCID仕込み量
反応物5-BromosalicylaldehydeHCID 72863—
反応物hydroxylamine-O-sulfonic acidHCID 76284—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物5-Bromo-1,2-benzoxazoleHCID 12003029—

反応条件

温度0 °C

反応手順

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)−

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737160B2
出典データセットuspto-grants-2010_06
ORD IDord-d2a564846363457bbd5a6780f7989129
出典メモuspto-grants-2010_06