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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182183Generated: October 31, 2026

Potassium Iodide → 1-(4-Methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonate

https://huagongshe.com/reaction/1182183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-Methyl-2-butanolHCID 6405—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-4'-methoxybutyrophenoneHCID 96414—
ReactantHCID 178418936HCID 178418936—
SolventDiisopropylether ethyl acetateHCID 22281796—
Product1-(4-Methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonateHCID 86607830—

Reaction Steps

10.6 g (50 mmol) 4-Chloro-1-(4-methoxy-phenyl)-butan-1-one, 20 ml 2-methyl-2-butanol, 5.2 g (75 mmol) 1H-[1,2,3]-triazole, 9.5 g (57 mmol) potassium iodide and 3.0 g (75 mmol) NaOH were stirred at 100° C. for 4 h. After removal of solvents in vacuo, the residue was partitioned between toluene and water. Washing of the toluene phase twice with water, drying over sodium sulphate and evaporation gave an oily residue that was dissolved in 80 ml diisopropyl ether/ethyl acetate (1:2). The solution was kept at 20° C. during the addition of 2.8 ml methanesulfonic acid and stirred at room temperature for 2 h. The formed precipitate was isolated, washed with cold diethyl ether and dried at 40° C. in vacuo to give 1-(4-methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonate. Yield: 2.25 g (13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288557B2
Source datasetuspto-grants-2007_10
ORD IDord-453b17ff653e438983191caf386e2e68
Source noteuspto-grants-2007_10