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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945361Generated: November 2, 2026

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

https://huagongshe.com/reaction/1945361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-Bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 58175487—
ReactantHCID 178527019HCID 178527019—
SolventAcetic AcidHCID 176—
Product2-Bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13h-indeno[1,2-b]anthraceneHCID 5817555076%

Reaction Steps

2-Bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol (5 g, 1 eq, 0.0075 mol), potassium iodide (12.45 g, 10 eq, 0.075 mol), and sodium hypophosphite (6 g, 5 eq, 0.037 mol) were placed in a flask, and acetic acid (200 ml) was added thereto. 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 a target compound (3.56 g, yield=76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08395144B2
Source datasetuspto-grants-2013_03
ORD IDord-75e49b012ecd4ca48f50631dd1b7437e
Source noteuspto-grants-2013_03