HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703353Generated: October 30, 2026
1H-1,2,4-Triazole → HCID 14403430, compound
https://huagongshe.com/reaction/703353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | 2-(2,4-Dichlorophenylethenyl)-2-(1-propylmercaptocyclopropyl) oxirane | HCID 54087481 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene ethylacetate | HCID 21584019 | — |
| Product | HCID 14403430 | HCID 14403430 | 26% |
Reaction Steps
A solution of 38.2 g (0.12 mol) of 2-(2,4-dichlorophenyl-ethenyl)-2-(1-propylmercaptocyclopropyl)-oxirane in 30 ml of dimethylformamide is added dropwise at 80° C. under a nitrogen atmosphere and with stirring to a mixture of 24 g (0.35 mol) of 1,2,4-triazole, 2.7 g (0.02 mol) of potassium tert.-butylate and 50 ml of dimethylformamide. The mixture is stirred for 6 hours at 80° C., then the solvent is stripped off under reduced pressure, and the residue is taken up in ethyl acetate/toluene, washed using water, dried over sodium sulphate and concentrated under reduced pressure. The residue remaining is chromatographed on silica gel using chloroform as eluant. In this manner, 12.1 g (26% of theory) of trans-4-(2,4-dichlorophenyl)-2-(1-propylmercaptocyclopropyl)-1-(1,2,4-triazol-1-yl)-but-3-en-2-ol are obtained in the form of an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983208 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-558a8957b80f4948ba5fbf4d3c06b592 |
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| Source note | uspto-grants-1991_01 |
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