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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623692Generated: October 26, 2026

5-Trifluoromethylthiophene-3-one → 4-methyl-2-[4-(trifluoromethyl)phenyl]-5-[[5-(trifluoromethyl)-3-thienyl]oxy]-2H-1,2,3-triazole

https://huagongshe.com/reaction/623692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Trifluoromethylthiophene-3-oneHCID 2760786—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-Methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborateHCID 90111332—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-methyl-2-[4-(trifluoromethyl)phenyl]-5-[[5-(trifluoromethyl)-3-thienyl]oxy]-2H-1,2,3-triazoleHCID 90111975—

Reaction Conditions

Temperature23 °C

Reaction Steps

Potassium tert-butoxide (0.30 g, 2.6 mmol) and 5-trifluoromethylthiophene-3-one (0.44 g, 2.6 mmol) were dissolved in acetonitrile (4 mL). A solution of crude 1-methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate (1:1) (i.e., the product of Example 1, Step B, 0.70 g, 2.0 mmol) in acetonitrile (4 mL) was added at once. The reaction mixture was stirred at 23° C. for 27 h. The reaction mixture was diluted with water (20 mL) and extracted with diethyl ether (2×25 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure. The crude residue was purified by chromatography on silica gel eluting with 0 to 5% ethyl acetate in hexanes to afford the title compound (0.105 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302999B2
Source datasetuspto-grants-2016_04
ORD IDord-3e1edb8ca99f4364b81bdc433ceda548
Source noteuspto-grants-2016_04