HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569705Generated: October 29, 2026
Sulfoxonium, trimethyl-, iodide (1:1) → HCID 13080456, compound
https://huagongshe.com/reaction/569705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | 3,3-Dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanone | HCID 100877 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13080456 | HCID 13080456 | 69.4% |
Reaction Steps
6 g (0.11 mol) of sodium methylate were introduced in portions into a suspension of 24 g (0.11 mol) of trimethylsulphoxonium iodide in 24 g of dimethylsulphoxide. 10 ml of tetrahydrofuran were also added, and the reaction mixture was then stirred for 5 hours at room temperature. Thereafter, a solution of 16.8 g (0.1 mol) of 1,2,4-triazol-1-yl-pinacolin in 100 ml of tetrahydrofuran was added dropwise, and the mixture was heated at 70° C. for 5 hours. The reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was dissolved in chloroform, and the solution was washed with water, dried over sodium sulphate, filtered and concentrated. 13.8 g of a 69.4% pure 2-tert.-butyl-2-(1,2,4-triazol-1-yl-methyl)-oxirane of refractive index nD20 =1.4872 were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734126 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-898029fc29b94891a58952066b824bc7 |
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| Source note | uspto-grants-1988_03 |
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