Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40406Generated: October 26, 2026

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

https://huagongshe.com/reaction/40406

Reaction equation

Participants

RoleNameHCIDCharge
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, 0.0075 mol), KI (12.45 g, 0.075 mol), and Sodium hypophosphite (6 g, 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 with distilled water, filtered, and purified by column chromatography to give 2-bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13H-indeno[1,2-b]anthracene (3.56 g, yield=76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08525158B2
Source datasetuspto-grants-2013_09
ORD IDord-20caf7a413a84dcaa1170aaff5e338f4
Source noteuspto-grants-2013_09