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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676414Generated: October 25, 2026

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

https://huagongshe.com/reaction/1676414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-PhenylanthraceneHCID 11766—
ReactantBromineHCID 24408—
ReactantThiosulfuric acid, disodium salt, monohydrateHCID 108762—
SolventCarbon TetrachlorideHCID 5943—
Product9-Bromo-10-phenyl-anthraceneHCID 415583689%

Reaction Steps

6.0 g (23.7 mmol) of 9-phenylanthracene was dissolved in 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 by a dropping funnel. After the dropping, stirring was conducted for 1 hour at room temperature. After reaction, a sodium thiosulfate water solution was added and the reaction was stopped. An organic layer was washed with an NaOH water solution and a saturated saline and dried with magnesium sulfate. After the natural filtration, it was concentrated, dissolved in toluene, and filtered through florisil, Celite (registered trademark), and alumina. The filtrate was concentrated and recrystallized by dichloromethane and hexane. Then, 7.0 g of a light-yellow solid of 9-bromo-10-phenylanthracene, which was the intended object, was obtained with a yield of 89% (synthetic scheme of (b-4)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003977B2
Source datasetuspto-grants-2011_08
ORD IDord-e7014530fe044d5db11395c7f2d02115
Source noteuspto-grants-2011_08