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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806192Generated: October 30, 2026

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

https://huagongshe.com/reaction/1806192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DiphenylisobenzofuranHCID 21649—
Reactant5-BromoacenaphthyleneHCID 12244403—
SolventO-XyleneHCID 7237—
Product3-Bromo-7,12-diphenylbenzo[k]fluorantheneHCID 1079098252.7%

Reaction Steps

200 ml of xylene were added to 5-bromoacenaphthylene (14.5 g, 62.8 mmol) and diphenylisobenzofuran (17.1 g, 63.3 mmol) and the mixture was stirred under reflux of xylene for 5 hours. After the mixture was cooled to room temperature, the solvent was distilled off. Then, 26 ml of trifluoroacetic anhydride and 260 ml of chloroform were added thereto, followed by stirring under reflux for 1 hour. After the mixture was cooled to room temperature, the solvent was distilled off. The obtained residue was purified by silica gel chromatography (mobile phase; toluene:heptane=1:3), whereby 16 g of 4-bromo-7,12-diphenylbenzo[k]fluoranthene were obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354788B2
Source datasetuspto-grants-2013_01
ORD IDord-fcb6199e435446129a53a77834d81844
Source noteuspto-grants-2013_01