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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1610784생성일: 2026년 10월 25일

2-Bromonaphthalene → 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol

https://huagongshe.com/reaction/1610784

반응식

참여 물질

역할이름HCID투입량
반응물2-BromonaphthaleneHCID 11372—
반응물2-BromoanthraquinoneHCID 221013—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diolHCID 2224716693%

반응 단계

To a solution of 2-bromonaphthalene (6.49 g, 31.3 mmol) in dry THF (50 ml) was added dropwise t-BuLi (18.4 ml of a 1.7 M solution in pentane) at −78° C. under nitrogen. After the mixture had been stirred for 30 min, 2-bromoanthraquinone (3.00 g, 10.4 mmol) was added at −78° C. The cooling bath was removed and the mixture was stirred for 2 hours at room temperature. The mixture was quenched with saturated aqueous ammonium chloride solution (50 ml) and extracted with ethyl ether (3×50 ml). The combined organic extracts were dried over MgSO4 and concentrated under vacuum. The crude product was slurried in petroleum ether, filtered off with suction, and washed with petroleum ether. After drying, the 2-bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol (5.30 g, 93%) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06984462B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-e36c353889f04976be3e3322e335d23f
출처 메모uspto-grants-2006_01