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HRID 382089作成日:2026年10月26日

P-Chloroacetophenone → 1-(3'-Methyl[1,1'-biphenyl]-4-yl)ethanone

https://huagongshe.com/reaction/382089

反応式

関与物質

役割名称HCID仕込み量
反応物P-ChloroacetophenoneHCID 7467—
反応物Cesium fluorideHCID 25953—
反応物3-Tolylboronic acidHCID 2733950—
触媒palladium(II) acetateHCID 167845—
触媒2,3',5-Trimethyl-1,1'-biphenylHCID 11041689—
溶媒1,4-DioxaneHCID 31275—
生成物1-(3'-Methyl[1,1'-biphenyl]-4-yl)ethanoneHCID 511295493%

反応手順

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (4.4 mg, 0.02 mmol, 2 mol %), ligand 2 [Example 1] (11.9 mg, 0.03 mmol, 3 mol %), 3-methylphenylboronic acid (204 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL), and 4-chloroacetophenone (0.13 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 chloride 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 1M 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 195 mg (93%) of a white solid.

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-082a34eed01047abb85f6381075a1d7b
出典メモuspto-grants-2001_10