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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 496944생성일: 2026년 10월 24일

Phenylboronic Acid → 2,6-Dimethylbiphenyl

https://huagongshe.com/ko/reaction/496944

반응식

참여 물질

역할이름HCID투입량
반응물Phenylboronic AcidHCID 66827—
반응물2-Bromo-m-xyleneHCID 68471—
반응물Potassium FluorideHCID 522689—
촉매palladium(II) acetateHCID 167845—
촉매2-(Di-tert-butylphosphino)biphenylHCID 2734215—
용매TetrahydrofuranHCID 8028—
생성물2,6-DimethylbiphenylHCID 13809079%

반응 단계

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromo-m-xylene (0.144 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at 65° C. until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 144 mg (79%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06946560B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-f614fd4d1e1a4e179b1cc44e44e05fda
출처 메모uspto-grants-2005_09