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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907076Generated: November 1, 2026

Bromosuccinimide → 10-(Biphenyl-4-yl)-2-bromo-9,10-dihydroacridine

https://huagongshe.com/reaction/1907076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromosuccinimideHCID 38309—
Reactant10-(Biphenyl-4-yl)-9,10-dihydroacridineHCID 18720419—
SolventChloroformHCID 6212—
Product10-(Biphenyl-4-yl)-2-bromo-9,10-dihydroacridineHCID 6752358077.7%

Reaction Steps

The obtained 10-(biphenyl-4-yl)-9,10-dihydroacridine (15.3 g, 45.9 mmol) was added with chloroform (500 ml), and then with bromosuccinimide (9.8 g, 55.1 mmol). The resultant solution was stirred at room temperature for 2 hours. After the reaction was completed, the resultant solution was washed with distilled water. Then, an organic layer was extracted and dried with sodium sulfate so as to remove the solvent. The residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/20)) to obtain 10-(biphenyl-4-yl)-2-bromo-9,10-dihydroacridine compound (white solid, 14.7 g, yield 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08597802B2
Source datasetuspto-grants-2013_12
ORD IDord-385169d1f60d4714b26b893d582ccc4a
Source noteuspto-grants-2013_12