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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606797Generated: October 30, 2026

Hydrogen Peroxide → 2-Fluoro-5-iodophenol

https://huagongshe.com/reaction/606797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant2-Fluoro-5-iodophenylboronic acidHCID 16217450—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-iodophenolHCID 46911832—

Reaction Steps

To a cooled solution of 2-fluoro-5-iodophenylboronic acid in tetrahydrofuran (200 mL) at 0° C. add an aqueous solution of 30% hydrogen peroxide (9.92 mL, 103 mmol) dropwise, stir 10 min, and add an aqueous 4 N solution of sodium hydroxide (1.78 mL, 7.12 mmol). Warm the reaction to room temperature and stir overnight. Add manganese dioxide (250 mg) to the reaction, stir 90 min and filter through fluted filter paper. Concentrate and partition the residue between diethyl ether and water. Separate the layers and sequentially wash the organic layer with water and an aqueous saturated solution of sodium chloride. Dry (sodium sulfate), filter and concentrate. Purify the resulting tan oil by silica gel chromatography, eluting with a gradient of 0:100 to 30:70 ethyl acetate:hexanes, to give the title compound as a yellow waxy solid (18.1 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-85b8cbf127b34f26b6a74e6cd07837fc
Source noteuspto-grants-2011_03