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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11194Generated: October 30, 2026

1,3-Diphenylisobenzofuran → 3-Bromo-7,12-diphenylbenzo[k]fluoranthene

https://huagongshe.com/reaction/11194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DiphenylisobenzofuranHCID 21649—
Reactant5-BromoacenaphthyleneHCID 12244403—
SolventTolueneHCID 1140—
Product3-Bromo-7,12-diphenylbenzo[k]fluorantheneHCID 1079098278.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

5 g (18.5 mmol) of diphenylisobenzofuran and 4.3 g (18.5 mmol) of 5-bromoacenaphthylene in toluene were agitated for 24 hours at the reflux temperature. The solvent was distilled off in vacuum, after which the residue was dissolved in 500 ml of acetic acid. An aqueous 40% hydrobromic acid solution, 50 cm3, was added to the solution, which was heated at 80° C. for one hour. After cooling to room temperature, the precipitate was collected by filtration. This was purified by silica gel chromatography using a mixture of toluene and hexane as an extracting solvent, yielding 7 g of 3-bromo-7,12-diphenylbenzo[k]fluoranthene having a yellowish white color.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07097917B1
Source datasetuspto-grants-2006_08
ORD IDord-cda3828502ec4ec5b4a279b75eb3511f
Source noteuspto-grants-2006_08