Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714414Generated: November 3, 2026

Iodine → 9-Iodo-10-phenylanthracene

https://huagongshe.com/reaction/1714414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
Reactant9-Bromo-10-phenyl-anthraceneHCID 4155836—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product9-Iodo-10-phenylanthraceneHCID 1495837383%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3.33 g (10 mmol) of 9-bromo-10-phenylanthracene was dissolved into 80 mL of tetrahydrofuran (abbr.: THF) and cooled to −78° C., and then 7.5 mL (12.0 mmol) of n-BuLi (1.6 mol/L) was dropped into the reaction solution using a dropping funnel and stirred for 1 hour. A solution in which 5 g (20.0 mmol) of iodine was dissolved in 20 mL of THF was dropped and further stirred for 2 hours at −78° C. After the reaction, an aqueous sodium thiosulfate solution was added to stop the reaction. An organic layer was washed with an aqueous sodium thiosulfate solution and a saturated sodium chloride solution and dried with magnesium sulfate. After natural filtration, the filtrate was concentrated, and the obtained solid was recrystallized with ethanol, thereby obtaining 3.1 g of objective 9-iodo-10-phenylanthracene as a light-yellow solid with a yield of 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795449B2
Source datasetuspto-grants-2010_09
ORD IDord-cc1c0232e1d8438e9f67d69c0a9e3e91
Source noteuspto-grants-2010_09