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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11745생성일: 2026년 10월 24일

1,10-Phenanthroline → 4,4'-Dibromo-N,N-diphenyl[1,1'-biphenyl]-2-amine

https://huagongshe.com/ko/reaction/11745

반응식

참여 물질

역할이름HCID투입량
반응물1,10-PhenanthrolineHCID 1318—
반응물IodobenzeneHCID 11575—
반응물Potassium HydroxideHCID 14797—
반응물5-Bromo-2-(4-bromophenyl)anilineHCID 4559420—
촉매Cuprous chlorideHCID 62652—
용매TolueneHCID 1140—
생성물4,4'-Dibromo-N,N-diphenyl[1,1'-biphenyl]-2-amineHCID 21976317835.7%

반응 단계

4,4′-Dibromo-2-amino-1,1′-biphenyl (16.35 g, prepared according to Libman and Slack (1951) J. Chem. Soc., p. 2588), iodobenzene (26.52 g, 0.13 mol), flake potassium hydroxide (22.4 g, 0.35 mol), 1,10-phenanthroline (0.45 g), copper (I) chloride (0.25 g), and toluene (30 ml) were charged into a flask and stirred at reflux for 15 hours. The dark reaction mixture was cooled to room temperature and diluted with 200 ml of toluene. The toluene solution was washed with DI water, dried with magnesium sulfate, and evaporated. The dark residue obtained was recrystallized trice from hexane/toluene (4:1 volume) to yield 10 grams of white crystals to yield the desired monomer. 1H NMR (CDCl3): δ=6.8–7.5, multiple peaks.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098297B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-709f53a743134d82ad7ff2bb00604b97
출처 메모uspto-grants-2006_08