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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426378Generated: October 25, 2026

Potassium Iodide → 2-Bromo-9,10-diphenylanthracene

https://huagongshe.com/reaction/426378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPhosphinic AcidHCID 4124402—
Reactant2-Bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diolHCID 23160218—
ReactantHCID 178418950HCID 178418950—
SolventAcetic AcidHCID 176—
Product2-Bromo-9,10-diphenylanthraceneHCID 2224716374%

Reaction Conditions

Temperature120 °C

Reaction Steps

7.55 g (16.95 mmol) of the obtained 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol, 5.06 g (30.51 mmol) of potassium iodide, 9.70 g (91.52 mmol) of sodium phosphinate monohydrate, and 50 mL of glacial acetic acid were put into a 500 mL three-neck flask, and the mixture was heated at 120° C. for 2 hours. Thereafter, 30 mL of 50% phosphinic acid was added to the mixture, and the mixture was stirred for 1 hour at 120° C. After the reaction, the mixture was washed with water, and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated. The residue was dissolved in toluene, and the solution was filtered through celite, Florisil, and then alumina. The filtrate was concentrated, and the residue was recrystallized with chloroform and hexane, giving 5.1 g of 2-bromo-9,10-diphenylanthracene as a light yellow solid in 74% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106392B2
Source datasetuspto-grants-2012_01
ORD IDord-cb04386157424ceeb290d55e35150671
Source noteuspto-grants-2012_01