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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085800Generated: October 26, 2026

Dimethyl Sulfate → 4-Chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxirane

https://huagongshe.com/reaction/1085800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant4-Chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketoneHCID 13366855—
SolventTetrahydrofuranHCID 8028—
Product4-Chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxiraneHCID 13366863—

Reaction Steps

9.6 g (0.044 mole) of trimethylsulphonium iodide are dissolved in 9.6 g (0.118 mole) of dimethyl sulphate under a nitrogen atmosphere. 5.2 g (0.044 mole) of potassium tert.-butylate are added at room temperature and the mixture is subsequently stirred at room temperature for 6 hours. A solution of 9.9 g (0.0397 mole) of 4-chlorophenyl 2-(1,2,4-triazol-1-yl)-prop-2-yl ketone in 16 ml of tetrahydrofuran is then added dropwise at room temperature. The reaction mixture is subsequently led at room temperature for 15 hours and under reflux for 4 hours, cooled and filtered. The filtrate is concentrated in vacuo, the residue is discharged onto water and the mixture is extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated in vacuo. 10.4 g (100% of theory) of 2-(4-chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxirane of refractive indes nD20 1.5388 are obtained. ##STR18##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011850
Source datasetuspto-grants-1991_04
ORD IDord-782f5a63f9364bd98bf0b215b0ba5e42
Source noteuspto-grants-1991_04