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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616933Generated: October 25, 2026

Sodium Iodide → 1-Ethoxy-3-fluoro-5-iodobenzene

https://huagongshe.com/reaction/1616933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTosylchloramideHCID 31388—
Reactant3-Ethoxy-5-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 44558175—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Ethoxy-3-fluoro-5-iodobenzeneHCID 67324085—

Reaction Steps

(3-Ethoxy-5-fluorophenyl)boronic acid (2.5 g, 0.014 mol) was dissolved in THF (30 mL) and a solution of sodium iodide (4.1 g, 0.028 mol) in H2O (15 mL) was added followed by a solution of chloramine T (7.8 g, 0.1 mol) in H2O (15 mL). After 20 h stirring, the reaction mixture was extracted with diethylether (3×50 mL). The organic layers were combined and the solvent was evaporated. The resulting residue was triturated with hexanes (3×) and the hexanes layers were combined. The solvent was evaporated to yield 1-fluoro-3-iodo-5-ethoxybenzene as an orange oil. The product was used in the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765779B2
Source datasetuspto-grants-2014_07
ORD IDord-d24e001545984dbd80bd1dc1c64c4c0d
Source noteuspto-grants-2014_07