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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1928667생성일: 2026년 10월 26일

Phenyl-1-naphthylamine → N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine

https://huagongshe.com/reaction/1928667

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl-1-naphthylamineHCID 7013—
반응물4,4'-DibromobiphenylHCID 7110—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매TolueneHCID 1140—
생성물N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amineHCID 1675531270%

반응 조건

온도90 °C

반응 단계

A mixture of 4,4′-dibromobiphenyl (8.46 g=27.4 mmol), Pd(OAc)2 (105 mg=0.18 mmol), dppf (253 mg=0.46 mmol), N-(1-naphthyl)aniline (2.0 g=9.13 mmol) and sodium t-butoxide (1.32 g=13.7 mmol) in dry toluene was placed in a three-necked flask under a nitrogen atmosphere and stirred at 90° C. for 15 h. After cooling, the reaction was quenched by adding water and then extracted by ethyl acetate. The organic layer was dried over anhydrous MgSO4 and evaporated under vacuum. The products were purified by a silica gel column eluted with hexane. White solid of compound 2N was obtained in 70% yield (2.86 g=6.37 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08183393B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-445ad050c76a4e5ca7eae9f41f26deb5
출처 메모uspto-grants-2012_05