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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271396Generated: October 25, 2026

Potassium Iodide → 1-[4-(4-{2-[2-(4-Trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazole

https://huagongshe.com/reaction/1271396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium MethoxideHCID 10942334—
Reactant4-(4-[1,2,3]Triazol-1-yl-butyl)phenolHCID 12109494—
Reactant4-Chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazoleHCID 69112977—
SolventMethanolHCID 887—
Product1-[4-(4-{2-[2-(4-Trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazoleHCID 69291825—

Reaction Steps

0.32 g (1.00 mmol) 4-Chloromethyl-2-[2-(4-trifluoromethylsulfanyl-phenyl)-vinyl]-oxazole, 0.217 g (1.00 mmol) 4-(4-[1,2,3]Triazol-1-yl-butyl)-phenol, 0.166 g (1.00 mmol) potassium iodide and 0.191 ml (1.00 mmol) of sodium methylate (30% in methanol) were added to 50.0 ml methanol and heated to reflux for 16 h. After removal of solvent and partitioning of the residue between 50 ml ethyl acetate and 15 ml water, the organic phase was washed with 10 ml water, 10 ml 0.1 N NaOH and twice 15 ml water, and dried over sodium sulfate. The solution was concentrated until crystallisation of the product started. After leaving for 1 h at room temperature the precipitate was isolated, washed with ether and dried at 40° C. in vacuo. Yield 0.11 g (18%) 1-[4-(4-{2-[2-(4-Trifluoromethylsulfanyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazole, m.p. 144–145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205325B2
Source datasetuspto-grants-2007_04
ORD IDord-9abd7797a62447028bd75506aeb7c04f
Source noteuspto-grants-2007_04