HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714413Generated: October 29, 2026
9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene
https://huagongshe.com/reaction/1714413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 9-Phenylanthracene | HCID 11766 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 9-Bromo-10-phenyl-anthracene | HCID 4155836 | 99.6% |
Reaction Steps
6.0 g (23.7 mmol) of 9-phenylanthracene was dissolved into 80 mL of carbon tetrachloride, and a solution in which 3.80 g (21.1 mmol) of bromine was dissolved in 10 mL of carbon tetrachloride was dropped into the reaction solution using a dropping funnel. After dropping, the solution was stirred for 1 hour at a room temperature. After the reaction, an aqueous sodium thiosulfate solution was added to stop the reaction. An organic layer was washed with an aqueous sodium hydroxide (NaOH) solution and a saturated sodium chloride solution and dried with magnesium sulfate. The mixture was naturally filtered, and a compound obtained by concentrating the filtrate was dissolved into toluene and filtered through florisil, Celite®, and alumina. The filtrate was concentrated and recrystallized with dichloromethane and hexane, thereby obtaining 7.0 g of objective 10-bromo-9-phenylanthracene as a light-yellow solid with a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795449B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-748c9982337847febbb61fbfb780f691 |
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| Source note | uspto-grants-2010_09 |
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