戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 519197作成日:2026年10月26日

Chloroacetyl chloride → 6-Bromo-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/519197

反応式

関与物質

役割名称HCID仕込み量
反応物Chloroacetyl chlorideHCID 6577—
反応物2-Amino-4-BromophenolHCID 351840—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物6-Bromo-2H-1,4-benzoxazin-3(4H)-oneHCID 1621814289%

反応条件

温度80 °C

反応手順

To a solution of 2-amino-4-bromophenol (25 g, 133.0 mmol), NaHCO3 (22.4 g, 266.0 mmol) in 4-methylpentan-2-one (50 mL) and water (50 mL) at 0° C. was added 2-chloroacetyl chloride (10.0 mL, 200.0 mmol) dropwise. The reaction mixture was stirred at 80° C. for 24 h then cooled to ambient temperature and filtered. The filtrate was washed with water (3×10 mL) and dried over anhydrous Na2SO4. After filtration, the organic phase was evaporated to give 6-bromo-4H-benzo[1,4]oxazin-3-one as a white solid (27 g, 89%). 1H NMR (CDCl3, 400 MHz): δ 8.49 (brs, 1H), 7.08 (dd, J=8.4 Hz, J=2.0 Hz, 1H), 6.93 (d, J=2.0 Hz, 1H), 6.87 (d, J=8.4 Hz, 1H), 4.61 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115151B2
出典データセットuspto-grants-2015_08
ORD IDord-d9310ec8cee44c6c80903629941d1172
出典メモuspto-grants-2015_08