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HRID 42384作成日:2026年10月23日

Sodium Hydroxide → 9-(4-(bicyclo[4.2.0]octa-1(6),2,4-trien-3-yl)butyl)-9-(4-(bicyclo[4.2.0]octa-1,3,5-trien-3-yl)butyl)-2,7-dibromo-9H-fluorene

https://huagongshe.com/ja/reaction/42384

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2,7-DibromofluoreneHCID 140073—
反応物3-(4-Bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-trieneHCID 58028492—
溶媒Dimethyl SulfoxideHCID 679—
生成物9-(4-(bicyclo[4.2.0]octa-1(6),2,4-trien-3-yl)butyl)-9-(4-(bicyclo[4.2.0]octa-1,3,5-trien-3-yl)butyl)-2,7-dibromo-9H-fluoreneHCID 58028498—

反応条件

温度80 °C

反応手順

To an oven-dried three-neck round-bottom flask under nitrogen, were added 25.97 g of 2,7-dibromofluorene, 32.06 g sodium hydroxide, 1.33 g KI, and 300 mL anhydrous DMSO. The 46 g 3-(4-bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-triene 300 mL anhydrous DMSO was added via cannula. The reaction was heated to 80° C. After 4 hours, the reaction was quenched by the addition of DI water (10 mL). The excess salt was removed by filtration. 500 mL Ethyl acetate was added, and extracted with DI water (3×300 mL) and brine (3×300 mL). The combined organic layer was dried over anhydrous magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was removed by rotary evaporation. The product (43 g) was purified by flash chromatography using hexane. The structure was confirmed by NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08535974B2
出典データセットuspto-grants-2013_09
ORD IDord-eef2893e491a4d5ab05d9efdcf8e0d14
出典メモuspto-grants-2013_09