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HRID 71706作成日:2026年10月25日

Water → 2-Bromo-1-(9-bromo-5,7-dihydro-dibenzo[c,e]oxepin-3-yl)-ethanone

https://huagongshe.com/reaction/71706

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-bromobutanimideHCID 67184—
反応物(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
反応物3,9-Dibromo-5,7-dihydrodibenzo[c,e]oxepineHCID 22316165—
触媒HCID 178418476HCID 178418476—
溶媒1,4-DioxaneHCID 31275—
生成物2-Bromo-1-(9-bromo-5,7-dihydro-dibenzo[c,e]oxepin-3-yl)-ethanoneHCID 5961029625.2%

反応条件

温度80 °C

反応手順

To the solution of 3,9-dibromo-5,7-dihydro-dibenzo[c,e]oxepine (416 mg, 1.2 mmol) and tributyl(ethoxyvinyl)stannane (878 μl, 2.6 mmol) in dioxane (6 ml) was added PdCl2(PPh3)2 (30 mg). The mixture was heated at 80° C. for 16 hours and was cooled to 0° C. Water (2 ml) was added, followed by slow addition of NBS (464 mg, 2.6 mmol) over 5 minutes period. The mixture was stirred at 0° C. for additional 40 minutes, and the solvent was removed under reduced pressure. The mixture was diluted with EtOAc, and was washed with water and brine and dried with sodium sulfate. Concentration and purification by flash column chromatography (hexane/EtOAc) gave 2-bromo-1-(9-bromo-5,7-dihydro-dibenzo[c,e]oxepin-3-yl)-ethanone (120 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822430B2
出典データセットuspto-grants-2014_09
ORD IDord-204059ad810a405b91c94d219535ca97
出典メモuspto-grants-2014_09