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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227871생성일: 2026년 10월 24일

Benzene, 2-bromo-1,4-dimethyl- → 2,5-Dimethylbiphenyl

https://huagongshe.com/ko/reaction/227871

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 2-bromo-1,4-dimethyl-HCID 11121—
반응물Phenylboronic AcidHCID 66827—
반응물Potassium FluorideHCID 522689—
촉매palladium(II) acetateHCID 167845—
촉매2-(Di-tert-butylphosphino)biphenylHCID 2734215—
용매TetrahydrofuranHCID 8028—
생성물2,5-DimethylbiphenylHCID 52250682%

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-p-xylene (0.138 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 room temperature 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 149 mg (82%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560582B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-0fc96fb876c146b2816281e659bf6391
출처 메모uspto-grants-2009_07