HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182183Generated: October 31, 2026
Potassium Iodide → 1-(4-Methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonate
https://huagongshe.com/reaction/1182183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-4'-methoxybutyrophenone | HCID 96414 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Solvent | Diisopropylether ethyl acetate | HCID 22281796 | — |
| Product | 1-(4-Methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonate | HCID 86607830 | — |
Reaction Steps
10.6 g (50 mmol) 4-Chloro-1-(4-methoxy-phenyl)-butan-1-one, 20 ml 2-methyl-2-butanol, 5.2 g (75 mmol) 1H-[1,2,3]-triazole, 9.5 g (57 mmol) potassium iodide and 3.0 g (75 mmol) NaOH were stirred at 100° C. for 4 h. After removal of solvents in vacuo, the residue was partitioned between toluene and water. Washing of the toluene phase twice with water, drying over sodium sulphate and evaporation gave an oily residue that was dissolved in 80 ml diisopropyl ether/ethyl acetate (1:2). The solution was kept at 20° C. during the addition of 2.8 ml methanesulfonic acid and stirred at room temperature for 2 h. The formed precipitate was isolated, washed with cold diethyl ether and dried at 40° C. in vacuo to give 1-(4-methoxy-phenyl)-4-[1,2,3]triazol-1-yl-butan-1-one methanesulfonate. Yield: 2.25 g (13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288557B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-453b17ff653e438983191caf386e2e68 |
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| Source note | uspto-grants-2007_10 |
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