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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640225Generated: November 1, 2026

Potassium Iodide → 2-Bromo-9,10-bis(4-fluorophenyl)anthracene

https://huagongshe.com/reaction/1640225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPhosphinic AcidHCID 4124402—
Reactant2-Bromo-9,10-bis(4-fluorophenyl)-9,10-dihydro-9,10-anthracenediolHCID 59211150—
ReactantHCID 178418950HCID 178418950—
SolventAcetic AcidHCID 176—
Product2-Bromo-9,10-bis(4-fluorophenyl)anthraceneHCID 5921110574%

Reaction Conditions

Temperature120 °C

Reaction Steps

8.32 (17.3 mmol) of 2-bromo-9,10-bis(4-fluorophenyl)-9,10-dihydro-9,10-anthracenediol, 5.17 g (31.1 mmol) of potassium iodide, 9.90 g (93.4 mmol) of sodium phosphinate monohydrate, and 50 mL of glacial acetic acid were put into a 200 mL three-neck flask, and the mixture was refluxed at 120° C. for 4 hours. Then, 20 mL of a 50% phosphinic acid was added into the reaction mixture, and the mixture was stirred for 1 hour at 120° C. After the reaction, the reaction mixture was washed with water, and the aqueous layer was extracted with ethyl acetate. This extracted solution was combined with the organic layer, and then dried with magnesium sulfate. After drying, the mixture was subjected to suction filtration, and the filtrate was concentrated. The obtained residue was dissolved in toluene, and filtered through Florisil, celite, and then alumina, and the filtrate was concentrated. The obtained residue was recrystallized with chloroform and hexane, giving 7.2 g of 2-bromo-9,10-bis(4-fluorophenyl)anthracene as light yellow powder in 74% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110980B2
Source datasetuspto-grants-2012_02
ORD IDord-f68b97c1f4f9458bb5be0965f76fc71d
Source noteuspto-grants-2012_02