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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380808Generated: November 3, 2026

Potassium Iodide → HCID 57500748, compound

https://huagongshe.com/reaction/2380808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3H-Thiopheno[2,3-d]1,2,3-triazin-4-oneHCID 13900098—
SolventAcetoneHCID 180—
ProductHCID 57500748HCID 5750074857.3%

Reaction Steps

To a solution of 3H-thiopheno[2,3-d]1,2,3-triazin-4-one (80 mg, 0.522 mmol) in acetone (50 mL) was added sequentially potassium carbonate (144 mg, 1.04 mmol), iodomethane (0.04 mL, 0.627 mmol) and potassium iodide (catalytic) at rt and the mixture was stirred at rt for 3 h. The solution was filtered and the solids were washed with acetone. Acetone was evaporated under reduced pressure, diluted with ice cold water and stirred for 10 min. The solution was extracted with chloroform (4×75 mL) and the combined CHCl3 layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (90:10) as eluents to give the product as an off-white solid (50 mg, 57%), mp 104-108° C. 1H NMR (400 MHz, DMSO-d6): δ 8.17 (1H, d, J=5.6 Hz), 7.64 (1H, d, J=5.6 Hz), 3.95 (3H, s); 13C NMR (100 MHz, CDCl3): δ 159.4, 153.9, 130.7, 125.6, 121.7, 37.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258119B2
Source datasetuspto-grants-2012_09
ORD IDord-32a1e37896f547a1aa1d0fbc0e39bb90
Source noteuspto-grants-2012_09