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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-PhenylanthraceneHCID 11766—
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
SolventCarbon TetrachlorideHCID 5943—
Product9-Bromo-10-phenyl-anthraceneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919773B2
Source datasetuspto-grants-2011_04
ORD IDord-0080101779af45f1b1b609442ef7f525
Source noteuspto-grants-2011_04