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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1755514생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1755514

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참여 물질

역할이름HCID투입량
반응물Phenyl-1-naphthylamineHCID 7013—
반응물4,4'-DibromobiphenylHCID 7110—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매TolueneHCID 1140—
생성물N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amineHCID 1675531262%

반응 조건

온도80 °C

반응 단계

A mixture of N-phenylnaphthalen-1-amine (4.41 g, 20 mmol), 4,4′-dibromo-1,1′-biphenyl (15 g, 48 mmol), sodium tert-butoxide (NaOBut) (4.8 g, 50 mmol) and Pd(dppf)Cl2 (0.44 g, 0.6 mmol) in anhydrous toluene (100 mL) was degassed and heated at 80° C. for about 10 hours. After cooling to RT, the mixture was poured into dichloromethane (400 mL) and stirred for about 30 min., then washed with brine (100 mL). The organic solution was collected and dried over Na2SO4, loaded on silica gel, and purified by flash column (hexanes to hexanes/ethyl acetate 90:1) to give a solid which was washed with methanol and dried under air to give a white solid Compound 4 (5.58 g, in 62% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09172051B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-bb1c2452679d4f3d8feb4e1f7f9f8309
출처 메모uspto-grants-2015_10