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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40412Generated: October 26, 2026

9-Bromophenanthrene → 9-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/40412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-BromophenanthreneHCID 11309—
Reactant9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dioneHCID 58175293—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product9-bromo-13,13-dimethyl-6,11-di(phenanthren-9-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 8665720664.2%

Reaction Steps

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, 9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione (9.67 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-di(phenanthren-9-yl)-11,13-dihydro6H-indeno[1,2-b]anthracene-6,11-diol (11.7 g, yield=64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08525158B2
Source datasetuspto-grants-2013_09
ORD IDord-d09c11998eef444088b4328b3090a3c8
Source noteuspto-grants-2013_09