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HRID 72565作成日:2026年10月26日

5-Bromo-2-chlorobenzoyl chloride → 1-[6-(5-Bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone

https://huagongshe.com/reaction/72565

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-chlorobenzoyl chlorideHCID 2756871—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物HCID 15171868HCID 15171868—
溶媒DichloromethaneHCID 6344—
生成物1-[6-(5-Bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanoneHCID 8665519779.3%

反応手順

To a stirred solution of 1-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-2,2,2-trifluoro-ethanone (6.5 g, 28.1 mmol) in dichloromethane (45 mL) was added 5-bromo-2-chlorobenzoyl chloride (8.54 g, 33.7 mmol) in dichloromethane (35 mL) and AlCl3 (5.61 g, 42.2 mmol) at 0° C. After 2 h, the reaction mixture was brought to room temperature and stirred overnight. The reaction was quenched by pouring over crushed ice and extracted with dichloromethane (2×50 mL). The organic layer was washed with aq. NaHCO3 (30 mL), H2O (20 mL), and the solvent evaporated to get the crude product which was purified by silica gel column chromatography to give 1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone (10.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828951B2
出典データセットuspto-grants-2014_09
ORD IDord-9e8d94565faf43948f9b5faeb25898aa
出典メモuspto-grants-2014_09