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HRID 40408Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromobenzeneHCID 7961—
EduktTetrahydrofuranHCID 8028—
Edukt9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dioneHCID 58175293—
EduktButyllithiumHCID 178418339—
Produkt9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 6738676763%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08525158B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-14aad029301941c69d94abba4b869465
Quellennotizuspto-grants-2013_09