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HRID 382087作成日:2026年10月26日

Cesium fluoride → 3,5-Dimethylbiphenyl

https://huagongshe.com/reaction/382087

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物1,4-DioxaneHCID 31275—
反応物Benzene, 1-bromo-3,5-dimethyl-HCID 136357—
反応物HCID 178419127HCID 178419127—
触媒palladium(II) acetateHCID 167845—
触媒2,3',5-Trimethyl-1,1'-biphenylHCID 11041689—
生成物3,5-DimethylbiphenylHCID 8692794%

反応手順

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1 mol %), ligand 2 [Example 1] (5.9 mg, 0.015 mmol, 1.5 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL) and 5-bromo-m-xylene (0.135 mL, 1.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (20 mL) and poured into a separatory funnel. The mixture was washed with 1 M NaOH (20 mL), and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 171 mg (94%) of a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06307087B1
出典データセットuspto-grants-2001_10
ORD IDord-a063042dab624e0391b6b2c29b70c448
出典メモuspto-grants-2001_10