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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Trifluoromethylthiophene-3-one | HCID 2760786 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-Methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate | HCID 90111332 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-methyl-2-[4-(trifluoromethyl)phenyl]-5-[[5-(trifluoromethyl)-3-thienyl]oxy]-2H-1,2,3-triazole | HCID 90111975 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302999B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-3e1edb8ca99f4364b81bdc433ceda548 |
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| Source note | uspto-grants-2016_04 |
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