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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40408생성일: 2026년 10월 24일

Bromobenzene → 9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol

https://huagongshe.com/ko/reaction/40408

반응식

참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물TetrahydrofuranHCID 8028—
반응물9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dioneHCID 58175293—
반응물ButyllithiumHCID 178418339—
생성물9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 6738676763%

반응 단계

Bromobenzene (8.5 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, 9-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 9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol (8.5 g, yield=63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08525158B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-14aad029301941c69d94abba4b869465
출처 메모uspto-grants-2013_09