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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503211Generated: October 31, 2026

Potassium Iodide → 3-[(2-Naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazine

https://huagongshe.com/reaction/1503211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-NaphtholHCID 8663—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Bromomethyl)[1,4]benzodioxino[2,3-c]pyridazineHCID 117691171—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-[(2-Naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazineHCID 8958464565.2%

Reaction Steps

To 3-(bromomethyl)[1,4]benzodioxino[2,3-c]pyridazine (500 mg) were added dimethylformamide (10 ml), potassium iodide (30 mg), potassium carbonate (750 mg) and 2-naphthylalcohol (290 mg), and the mixture was stirred at room temperature for 24 hr. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with 1M aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, and the residue was washed with diethyl ether and the resulting solid was filtered and dried under reduced pressure to give 3-[(2-naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazine (400 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212147B2
Source datasetuspto-grants-2015_12
ORD IDord-e3dbc379b74e477098d14e3a13ff124f
Source noteuspto-grants-2015_12