HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981542Generated: November 1, 2026
1H-1,2,4-Triazole → HCID 15593720, compound
https://huagongshe.com/reaction/981542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20070410 | HCID 20070410 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15593720 | HCID 15593720 | 31.9% |
Reaction Steps
To a solution of 2-(4-fluorophenyl)-2-[2-(1H-1,2,4-triazol-1-yl)prop-2-yl]oxirane (1.0 g, 4.0 mMole) in dimethylformamide (50 ml) were added 1,2,4-triazole (0.56 g., 8.0 mMole) and anhydrous potassium carbonate (0.56 g, 4.0 mMole). Heating at 80°, with stirring, was carried out for 19 hours. The solvent was then evaporated, water (75 ml) was added, and the mixture was extracted with methylene chloride (3×50 ml.). The combined organic extracts were washed with water (3×30 ml), dried over anhydrous magnesium sulphate, and evaporated to an impure gum (1.15 g). Purification of the gum was carried out using a flash column of Merck "Kieselgel 60" (Trademark) 230-400 mesh silica eluting with methylene chloride and 5% methanol in methylene chloride. The appropriate fractions on evaporation gave a solid which was recrystallised from diisopropylether and isopropyl alcohol giving the title compound, 0.4 g., m.p. 156°-158° (31.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992454 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-4e1d4844929742c88c03586c70d1017a |
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| Source note | uspto-grants-1991_02 |
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