Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481470Generated: October 30, 2026

Methyl iodide → 1H-1,2,4-Triazole-1-ethanol, alpha-(1-chlorocyclopropyl)-alpha-((2-chlorophenyl)methyl)-5-(methylthio)-

https://huagongshe.com/reaction/481470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178520209HCID 178520209—
SolventAcetonitrileHCID 6342—
Product1H-1,2,4-Triazole-1-ethanol, alpha-(1-chlorocyclopropyl)-alpha-((2-chlorophenyl)methyl)-5-(methylthio)-HCID 1850675595%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 3.43 g (10 mmol) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(5-mercapto-1,2,4-triazol-1-yl)-propan-2-ol, 20 ml of absolute acetonitrile and 1.38 g of (10 mmol) of potassium carbonate is treated with 0.93 ml (15 mmol) of methyl iodide and the mixture is stirred at 40° C. for 5 hours. The reaction mixture is then treated with saturated, aqueous sodium carbonate solution and extracted repeatedly using ethyl acetate. The combined organic phases are dried over sodium sulphate and concentrated under reduced pressure. In this manner, 3.4 g (95% of theory) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(5-methylthio-1,2,4-triazol-1-yl)-propan-2-ol are obtained in the form of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789430
Source datasetuspto-grants-1998_08
ORD IDord-faca5f74a0df44b584eea3d993d30686
Source noteuspto-grants-1998_08