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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113888Generated: November 4, 2026

Potassium Iodide → 1-[2-(2-Methyl-4-{2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-benzyloxy)-ethyl]-1H-[1,2,3]triazole

https://huagongshe.com/reaction/2113888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant4-Chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazoleHCID 69112977—
Reactant3-Methyl-4-(2-[1,2,3]triazol-1-yl-ethoxymethyl)-phenolHCID 69291015—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-[2-(2-Methyl-4-{2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-benzyloxy)-ethyl]-1H-[1,2,3]triazoleHCID 69292312—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 201 mg (0.86 mmol) 3-methyl-4-(2-[1,2,3]triazol-1-yl-ethoxymethyl)-phenol and 169 mg (0.52 mmol) cesium carbonate in 10 ml 2-butanone was stirred at 60° C. for 30 minutes, then 275 mg (0.86 mmol) 4-chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazole and 143 mg (0.86 mmol) potassium iodide were added and stirring was continued overnight. After evaporation, the residue was mixed with aqueous NaOH (1N) and extracted with ethyl acetate. The combined extracts were dried, evaporated and the product purified on silica (ethyl acetate) to yield 280 mg (63%) of the title as a white solid melting at 102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432291B2
Source datasetuspto-grants-2008_10
ORD IDord-991d50051a914041bd55804bc9adf43a
Source noteuspto-grants-2008_10