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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40408Generated: October 25, 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/reaction/40408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantTetrahydrofuranHCID 8028—
Reactant9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dioneHCID 58175293—
ReactantButyllithiumHCID 178418339—
Product9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 6738676763%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08525158B2
Source datasetuspto-grants-2013_09
ORD IDord-14aad029301941c69d94abba4b869465
Source noteuspto-grants-2013_09