Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075612Generated: November 2, 2026

Iodine → 9-Iodo-10-phenylanthracene

https://huagongshe.com/reaction/2075612

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

After 3.33 g (10 mmol) of 9-bromo-10-phenylanthracene was dissolved in 80 mL of tetrahydrofuran (abbreviation: THF) and cooled to −78° C., 7.5 mL (12.0 mmol) of n-BuLi (1.6 mol/L) was dropped through a dropping funnel into the reaction solution, and the mixture was stirred for one hour. Subsequently, a solution of 5 g (20.0 mmol) of iodine dissolved in 20 mL of THF was dropped, and the solution was further stirred at −78° C. for two hours. After the reaction, a sodium thiosulfate aqueous solution was added to stop the reaction. An organic layer was washed with a sodium thiosulfate aqueous solution and saturated saline and dried with magnesium sulfate. After the solution was filtered naturally, the filtrate was concentrated and recrystallized with ethanol; thus, 3.1 g of a light-yellow solid of 9-iodo-10-phenylanthracene as a target matter was obtained with a yield of 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919773B2
Source datasetuspto-grants-2011_04
ORD IDord-d32c3af671e342858e1a7ed35058e50a
Source noteuspto-grants-2011_04