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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584748Generated: October 30, 2026

Ethyl Acetate → HCID 10156604, compound

https://huagongshe.com/reaction/584748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant1,1,1-Trifluoro-2-iodoethaneHCID 67709—
ReactantHCID 178489016HCID 178489016—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10156604HCID 1015660445.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-(4-methoxyphenyl)-1-(6-methoxypyridin-3-yl)-1H-1,2,4-triazol-3-ol (300 mg, 1.01 mmol), potassium carbonate (417 mg, 3.02 mmol), and 2-iodo-1,1,1-trifluoroethane (0.496 mL, 5.03 mmol) in dimethyl sulfoxide (1.5 mL) were heated at 100° C. for 1 hour. After cooling, ice water and ethyl acetate were poured into the mixture and the organic layer was separated, washed with brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography (toluene-ethyl acetate 8:1) The desired product was washed with hexane to give 2-methoxy-5-(5-(4-methoxyphenyl)-3-(2,2,2-trifluoroethoxy)-1H-1,2,4-triazol-1-yl)pyridine (175 mg, 45.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927230B2
Source datasetuspto-grants-2005_08
ORD IDord-b4cea31b056f43359aed943f4e5f596f
Source noteuspto-grants-2005_08