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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012678Generated: November 2, 2026

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

https://huagongshe.com/reaction/1012678

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977869B2
Source datasetuspto-grants-2011_07
ORD IDord-03e769965f464c9e86ad36e1eae50bea
Source noteuspto-grants-2011_07