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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079153Generated: October 25, 2026

Sodium Iodide → 6-bromo-8-ethoxy-4H-benzo[1,3]dioxine

https://huagongshe.com/reaction/2079153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantBromochloromethaneHCID 6333—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-{3-[(4-carbamimidoylphenylamino)-(2-fluoro-4,5-dimethoxyphenyl)methyl]5-oxo-4,5-dihydro-[1,2,4]triazol-1-yl}benzoic Acid TrifluoroacetateHCID 136337083—
SolventEthyl AcetateHCID 8857—
Product6-bromo-8-ethoxy-4H-benzo[1,3]dioxineHCID 67096800—

Reaction Steps

To a solution of this compound in 40 ml of DMF there was added 1g of sodium hydride (60% oily suspension) while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After then adding 1 ml of bromochloromethane and 0.25 g of sodium iodide to the reaction mixture, it was stirred at 80° C. for 6 hours under a hydrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give 6-bromo-8-ethoxy-4H-benzo[1,3]dioxine (1.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928228B2
Source datasetuspto-grants-2011_04
ORD IDord-035d2348da454e09b4cd0f7fbaefe427
Source noteuspto-grants-2011_04