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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227852생성일: 2026년 10월 23일

4-Chlorotoluene → 4-Methylbiphenyl

https://huagongshe.com/ko/reaction/227852

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorotolueneHCID 7810—
반응물Cesium fluorideHCID 25953—
반응물1,4-DioxaneHCID 31275—
반응물HCID 178419127HCID 178419127—
촉매palladium(II) acetateHCID 167845—
촉매2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthylHCID 4368621—
생성물4-MethylbiphenylHCID 1256693%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560582B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-a7e18cfdb83e4d6996b0398a3246b81a
출처 메모uspto-grants-2009_07