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HRID 638774作成日:2026年10月27日

Toluene → 1,4-Phenylenebis(9,9-dimethylfluorene)

https://huagongshe.com/reaction/638774

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物1,4-Benzenediboronic acidHCID 230478—
反応物2-iodo-9,9-dimethyl-9H-fluoreneHCID 11023630—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1,4-Phenylenebis(9,9-dimethylfluorene)HCID 86606722—

反応条件

温度80 °C

反応手順

6.94 g (21.7 mmol) of 2-iodo-9,9-dimethylfluorene and 1 g (7.25 mmol) of 1,4-phenylenebis(boronic acid) were dissolved and agitated under nitrogen flow in the mixed solvent (120 ml of degassed toluene and 60 ml of ethanol), and 145 ml of sodium carbonate solution which was prepared by dissolving 30 g of anhydrous sodium carbonate in 150 ml of water was added dropwise thereto. After agitating for 30 minutes, 840 mg (0.727 mmol) of tetrakis(triphenylphosphine) palladium was added. Heating with agitation was carried out on the oil bath heated at 80° C. for about 3 hours. After cooling the reaction solution to room temperature, 50 ml of water and 50 ml of ethyl acetate were added, the aqueous layer and the organic layer were separated, the aqueous layer was further extracted with toluene and ethyl acetate, and the extract combined with the above organic layer was dried over magnesium sulfate. The solvent was evaporated, the residual substance was refined by silica gel column chromatography (toluene:hexane=1:2), and 3.02 g of 1,4-phenylenebis(9,9-dimethylfluorene) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691491B2
出典データセットuspto-grants-2010_04
ORD IDord-bf3eff5b1cc24aa6936fc31ffe04ca19
出典メモuspto-grants-2010_04