돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227873생성일: 2026년 10월 25일

4'-Bromoacetanilide → N-Acetyl-4-aminobiphenyl

https://huagongshe.com/reaction/227873

반응식

참여 물질

역할이름HCID투입량
반응물4'-BromoacetanilideHCID 7683—
반응물Phenylboronic AcidHCID 66827—
반응물Potassium FluorideHCID 522689—
촉매palladium(II) acetateHCID 167845—
촉매2-(Di-tert-butylphosphino)biphenylHCID 2734215—
생성물N-Acetyl-4-aminobiphenylHCID 1999886.2%

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, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 4′-bromoacetanilide (214 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was 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 182 mg (86%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560582B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-7f9e88ff24594db1b6115af7ca086cf9
출처 메모uspto-grants-2009_07