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HRID 253111作成日:2026年10月25日

Bromobenzene → Ethyl 3,4-dihydro-4-phenyl-2H-1,4-benzoxazine-2-carboxylate

https://huagongshe.com/reaction/253111

反応式

関与物質

役割名称HCID仕込み量
反応物BromobenzeneHCID 7961—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 3,4-dihydro-4-phenyl-2H-1,4-benzoxazine-2-carboxylateHCID 86614014—

反応条件

温度100 °C

反応手順

Tris(dibenzylideneacetone)dipalladium (0) (4.3 mg, 0.0046 mmol), xantphos (8.2 mg, 0.014 mmol), and bromobenzene (40 □L, 0.381 mmol) were added to a solution of (±)-ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (65 mg, 0.31 mmol) in dioxane (2.5 mL). The solids were allowed to dissolve, and cesium carbonate (143 mg, 0.44 mmol) was added, and the suspension was stirred at 100° C. for 24 h. The mixture was cooled to ambient temperature, diluted with water (20 mL), and the product was extracted with 67% EtOAc/hexane (3×25 mL). The organic layers were combined, dried over sodium sulfate, and concentrated. Purification of the crude concentrate by flash column chromatography using 15% EtOAc/hexane afforded the title compound. MS m/z: 284 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872009B2
出典データセットuspto-grants-2011_01
ORD IDord-378c8d6cc1b242259dac99d498f4cb3c
出典メモuspto-grants-2011_01