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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40407생성일: 2026년 10월 25일

9-Bromophenanthrene → 2-bromo-13,13-dimethyl-6,11-di(phenanthren-9-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol

https://huagongshe.com/reaction/40407

반응식

참여 물질

역할이름HCID투입량
반응물9-BromophenanthreneHCID 11309—
반응물2-Bromo-13,13-dimethyl-6H-indeno(1,2-b)anthracene-6,11(13H)-dioneHCID 58175361—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-bromo-13,13-dimethyl-6,11-di(phenanthren-9-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 8738087072%

반응 단계

9-bromophenanthrene (13.88 g, 0.054 mol) was placed in a flask, and THF (200 ml) was added thereto. After dissolution, n-BuLi (38.4 ml, 0.06 mol) was gradually added at −780, and the reaction mixture was stirred for one hour at a maintained temperature. Then, 2-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione (10 g, 0.024 mol) was added and the reaction mixture was stirred at room temperature for 12 hours. After the reaction was terminated, the reaction solution was washed with distilled water, extracted with ethyl acetate, and purified by column chromatography to give, 2-bromo-13,13-dimethyl-6,11-di(phenanthren-9-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol (13.1 g, yield=72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08525158B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0479e1595a5c4f09821c7eed8bc394c9
출처 메모uspto-grants-2013_09