HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368899Generated: October 26, 2026
1H-1,2,4-Triazole → (2S,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol
https://huagongshe.com/reaction/368899
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-ol | HCID 10867332 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2S,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol | HCID 9816851 | 38% |
Reaction Steps
To an ice cooled suspension of anhydrous K2CO3 (0.691 g, 0.005 mole) in N,N-dimethylformamide (7 ml), 1H-1,2,4-triazole (0.345, 0.005 mole) was added in small portions under art atmosphere of nitrogen. The mixture was slowly brought to room temperature and a solution of compound 7c (2R, 3S)-3-(2,4-Difluorophenyl)-3,4-epoxy-2-butanol (0.5 g, 0.0025 mole) in N,N-dimethylformamide (1 ml) was added. The resulting mixture was heated at 80° C. for 2 hours. The solvent was removed under reduced pressure and 25 g of crushed ice was added to the residue. The so formed mixture was extracted with ethyl acetate (50 ml, 2×25 ml). The combined organic layers were washed with water (10 ml) brine (25 ml) and dried over MgSO4. The solvent was removed in vacuo and the residue was chromatographed on silica gel. Elution with methanol in chloroform (0% -3%) gave the title compound 9c as an amorphous solid (0.26 g, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133485 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-feb19ed6c85c434cbda9a14ba43464e7 |
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| Source note | uspto-grants-2000_10 |
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