HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360744Generated: October 30, 2026
9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene
https://huagongshe.com/reaction/2360744
Participants
| Role | Name | HCID | Charge |
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| 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 dripped through a dropping funnel into the reaction solution. After the dripping, 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 a saturated saline solution 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 that was an object was obtained (yield: 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686159B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-c15033fb9852448ca0ea1e3c99d25cd0 |
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| Source note | uspto-grants-2014_04 |
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