HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398159Generated: October 26, 2026
Methanol → 1-(4-bromo-2-fluorophenyl)-3-methyl-1H-1,2,4-triazole
https://huagongshe.com/reaction/1398159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 609902 | HCID 609902 | — |
| Reactant | Methylethanimidothioate hydroiodide | HCID 11680130 | — |
| Product | 1-(4-bromo-2-fluorophenyl)-3-methyl-1H-1,2,4-triazole | HCID 66607884 | — |
Reaction Steps
To a mixture of (4-bromo-2-fluorophenyl)hydrazine (3.4 g) in methanol (25 mL) was added methyl ethanimidothioate hydroiodide (3.6 g), and the mixture was stirred at room temperature for 40 min. The solvent was evaporated under reduced pressure. To a mixture of the obtained residue in toluene (20 mL) were added methyl orthoformate (15 mL) and pyridine (15 mL), and the mixture was stirred at 100° C. for 9 hr. The reaction mixture was allowed to cool to room temperature, and diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, the organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (3.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901309B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-271d6b8f16ff4bcba2cd52f11b8f2ea2 |
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| Source note | uspto-grants-2014_12 |
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