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HRID 227852作成日:2026年10月26日

4-Chlorotoluene → 4-Methylbiphenyl

https://huagongshe.com/reaction/227852

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorotolueneHCID 7810—
反応物Cesium fluorideHCID 25953—
反応物1,4-DioxaneHCID 31275—
反応物HCID 178419127HCID 178419127—
触媒palladium(II) acetateHCID 167845—
触媒2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthylHCID 4368621—
生成物4-MethylbiphenylHCID 1256693%

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 %), 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 4-chlorotoluene (0.12 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 157 mg (93%) of a glassy solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560582B2
出典データセットuspto-grants-2009_07
ORD IDord-a7e18cfdb83e4d6996b0398a3246b81a
出典メモuspto-grants-2009_07