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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71130Generated: October 26, 2026

Methanol → 1-(4-bromo-2-fluorophenyl)-3-methyl-1H-1,2,4-triazole

https://huagongshe.com/reaction/71130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 609902HCID 609902—
ReactantMethylethanimidothioate hydroiodideHCID 11680130—
Product1-(4-bromo-2-fluorophenyl)-3-methyl-1H-1,2,4-triazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822699B2
Source datasetuspto-grants-2014_09
ORD IDord-9dec70ab15444c42849a5ed0a6bae456
Source noteuspto-grants-2014_09