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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623687Generated: October 26, 2026

Ethyl Acetate → 4-Methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole 1-oxide

https://huagongshe.com/reaction/623687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-(Trifluoromethyl)phenylhydrazineHCID 136200—
ReactantIsonitrosoacetoneHCID 6399095—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product4-Methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole 1-oxideHCID 9010948278.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirred solution of anti-pyruvic aldehyde 1-oxime (2.67 g, 30.7 mmol) in diethyl ether (50 mL) was added 4-(trifluoromethyl)phenylhydrazine (5.40 g, 30.7 mmol). The reaction mixture was stirred at 23° C. for 2 h, then concentrated under reduced pressure. The crude residue was dissolved in 15% aqueous pyridine (150 mL). A solution of copper(II) sulfate pentahydrate (15.31 g, 61.3 mmol) in water (75 mL) was added at once. The resulting mixture was stirred at reflux for 17 h, then cooled to 0° C. Ethyl acetate (100 mL) was added and the mixture was filtered through Celite® diatomaceaous filter aid. The layers were separated, and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with 1.0 M aqueous hydrochloric acid (3×50 mL). The organic layer was dried (MgSO4), filtered, and evaporated under reduced pressure. The residue was purified by chromatography on silica gel, eluting with 0 to 50% ethyl acetate in hexanes, to afford the title compound (5.84 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302999B2
Source datasetuspto-grants-2016_04
ORD IDord-5833b272dbd04ea38ed76cf8e55d1e8c
Source noteuspto-grants-2016_04