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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546650Generated: October 26, 2026

9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene

https://huagongshe.com/reaction/546650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-PhenylanthraceneHCID 11766—
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
SolventCarbon TetrachlorideHCID 5943—
Product9-Bromo-10-phenyl-anthraceneHCID 415583687.4%

Reaction Steps

20.8 g (81.7 mmol) of 9-phenylanthracene and 300 mL of carbon tetrachloride were put into a 500 mL three-necked flask. A solution obtained by dissolving 13.1 g (81.7 mmol) of bromine in 5.00 mL of carbon tetrachloride was dropped into the mixture. After the dropping was completed, the reaction solution was stirred at room temperature for 3 hours to be reacted. Then, about 100 mL of a sodium thiosulfate solution was added to the reaction solution to complete the reaction. An organic layer of the mixture was washed with water and dried over magnesium sulfate. After the drying, the mixture was subjected to suction filtration, and the filtrate was condensed to obtain a solid. The obtained solid was recrystallized by a mixed solvent of chloroform and hexane; then 23.8 g of objective 9-bromo-10-phenylanthracene was obtained as a light yellow powdered solid in a yield of 71%. A synthetic scheme of 9-bromo-10-phenylanthracene is illustrated below (synthetic scheme b-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935854B2
Source datasetuspto-grants-2011_05
ORD IDord-f9f67f0bbb5f49fcbd76d2eeafebd004
Source noteuspto-grants-2011_05