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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Diphenylisobenzofuran | HCID 21649 | — |
| Reactant | 5-Bromoacenaphthylene | HCID 12244403 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Bromo-7,12-diphenylbenzo[k]fluoranthene | HCID 10790982 | 78.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07097917B1 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-cda3828502ec4ec5b4a279b75eb3511f |
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| Source note | uspto-grants-2006_08 |
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