HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075611Generated: November 2, 2026
9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene
https://huagongshe.com/reaction/2075611
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 | — |
Reaction Steps
After 6.0 g (23.7 mmol) of 9-phenylanthracene was dissolved in 80 mL of carbon tetrachloride, a solution of 3.80 g (21.1 mmol) of bromine dissolved in 10 mL of carbon tetrachloride was dropped through a dropping funnel into the reaction solution. After the dropping, the solution was stirred at room temperature for one hour After the reaction, a sodium thiosulfate aqueous solution was added to stop the reaction. An organic layer was washed with a sodium hydroxide (NaOH) aqueous solution and saturated saline and dried with magnesium sulfate. After the solution was filtered naturally, the filtrate was concentrated, dissolved in toluene, and filtered through Florisil, Celite, and alumina. When the filtrate was concentrated and recrystallized with dichloromethane and hexane, 7.0 g of a light-yellow solid of 10-bromo-9-phenylanthracene, which is a target matter, was obtained with a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919773B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-0080101779af45f1b1b609442ef7f525 |
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| Source note | uspto-grants-2011_04 |
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