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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854683Generated: October 26, 2026

Potassium Iodide → 1-[2-(4-{2-[(e)-2-(4-Trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1h-[1,2,3]triazole

https://huagongshe.com/reaction/854683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant4-Chloromethyl-2-[2-(4-trifluoromethyl-phenyl)-vinyl]-thiazoleHCID 69428679—
Reactant4-(4-[1,2,3]Triazol-1-ylmethyl-oxazol-2-yl)-phenolHCID 136355231—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-[2-(4-{2-[(e)-2-(4-Trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1h-[1,2,3]triazoleHCID 1120299467.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.1212 g (0.50 mmol) 4-(4-[1,2,3]triazol-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 0.152 g (0.50 mmol) 4-chloromethyl-2-[2-(4-trifluoromethyl-phenyl)-vinyl]-thiazole 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 201 mg raw material which was recrystallised from ethanol to yield 171 mg (67%) 1-[2-(4-{2-[(E)-2-(4-trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1H-[1,2,3]triazole as white crystals melting at 179-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259262B2
Source datasetuspto-grants-2007_08
ORD IDord-b1d742f4d56648759057574e28f1270b
Source noteuspto-grants-2007_08