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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40410Generated: October 26, 2026

Potassium Iodide → 9-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13H-indeno[1,2-b]anthracene

https://huagongshe.com/reaction/40410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant9-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 58175336—
ReactantHCID 178527019HCID 178527019—
SolventAcetic AcidHCID 176—
Product9-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13H-indeno[1,2-b]anthraceneHCID 5817528971%

Reaction Steps

9-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol (11.87 g, 0.018 mol), Potassium iodide (29.88 g, 0.18 mol), and Sodium hypophosphite (35.63 g, 0.297 mol) were placed in a flask, and were suspended in acetic acid (300 ml). The reaction mixture was stirred for five hours while heating. After the reaction was terminated, the reaction solution was added to an excess of distilled water. The resultant solid was washed, filtered and purified by column chromatography to give 9-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13H-indeno[1,2-b]anthracene (8 g, yield=71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08525158B2
Source datasetuspto-grants-2013_09
ORD IDord-f685fddc85a44e5698379e61393ca7bf
Source noteuspto-grants-2013_09