Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | 1-(3-Bromo-1-methyl-1H-1,2,4-triazol-5-YL)ethan-1-OL | HCID 90017669 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 84671998 | HCID 84671998 | 58.4% |
Reaction Steps
A solution of 1-(3-bromo-1-methyl-1H-1,2,4-triazol-5-yl)ethanol (1.639 g, 7.95 mmol, Eq: 1.00) and pyridine (944 mg, 965 μl, 11.9 mmol, Eq: 1.5) in dichloromethane (237 ml) was cooled to 0° C. then Dess-Martin periodinane (15% in dichloromethane, 24.7 g, 8.75 mmol, Eq: 1.1) was added. The resulting mixture was stirred for 4 hours at 0° C. under nitrogen atmosphere. The mixture was diluted with dichloromethane and washed with sat. sodium hydrogen carbonate. The organic layer was separated, dried over magnesium sulfate, filtrated and evaporated. The crude material was applied on silica gel and purified by flash chromatography over a 20 g silica gel column using dichloromethane/methanol 0-3% & 5% NH3 as eluent affording 1-(5-bromo-2-methyl-2H-[1,2,4]triazol-3-yl)-ethanone (948 mg, 58.4%) as a white solid. MS: m/z=203 (EI)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394311B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-0d9657c11442411ab611afac4dc96f33 |
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| Source note | uspto-grants-2016_07 |
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