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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854691Generated: October 25, 2026

Potassium Iodide → 1-[2-(4-{2-[(E)-2-(-4-Trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1H-imidazole

https://huagongshe.com/reaction/854691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant4-Chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazoleHCID 69112977—
Reactant4-(4-Imidazol-1-ylmethyl-oxazol-2-yl)-phenolHCID 136343191—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-[2-(4-{2-[(E)-2-(-4-Trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1H-imidazoleHCID 1120325142%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.121 g (0.50 mmol) 4-(4-imidazol-1-ylmethyl-oxazol-2-yl)-phenol and 0.10 g (0.30 mmol) cesium carbonate in 10 ml butanone was stirred at 60° C. for 30 min, then 0.160 g (0.50 mmol) 4-chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazole and 0.083 g (0.50 mmol) potassium iodide were added and stirring at 60° C. continued over night. After evaporation, 15 ml water was added and the mixture extracted with two portions of 15 ml ethyl acetate. The combined organic layers were washed with 1N sodium hydroxide and water, dried over sodium sulfate and evaporated to give 110 mg (42%) of the title compound as light brown crystals melting at 144-145° C. (from 2-propanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259262B2
Source datasetuspto-grants-2007_08
ORD IDord-db29745e47964eb7b87909a6d4ab4a93
Source noteuspto-grants-2007_08