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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503210Generated: October 25, 2026

Sodium Iodide → 3-Iodo[1,4]benzodioxino[2,3-c]pyridazine

https://huagongshe.com/reaction/1503210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHydrogen iodideHCID 24841—
Reactant3-Chlorobenzo[5,6][1,4]dioxino[2,3-c]pyridazineHCID 12213466—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product3-Iodo[1,4]benzodioxino[2,3-c]pyridazineHCID 8958464027.6%

Reaction Conditions

Temperature140 °C

Reaction Steps

Under an argon atmosphere, 3-chloro[1,4]benzodioxino[2,3-c]pyridazine (5.0 g), sodium iodide (6.79 g) and hydrogen iodide (55%) (57.98 g) were added and the mixture was stirred at 140° C. for 1 hr. The reaction mixture was diluted with ethyl acetate and aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted. The organic layer was dried over anhydrous sodium sulfate, and the solvent was concentrated under reduced pressure to give 3-iodo[1,4]benzodioxino[2,3-c]pyridazine (1.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212147B2
Source datasetuspto-grants-2015_12
ORD IDord-aaa65a21822d49259296ebf3080a7d51
Source noteuspto-grants-2015_12