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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497394Generated: October 31, 2026

1-Butanol → 5-bromo-4-fluoro-2,3-dimethyl-2H-indazole

https://huagongshe.com/reaction/1497394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-(3-Bromo-2,6-difluorophenyl)ethanoneHCID 68110119—
Product5-bromo-4-fluoro-2,3-dimethyl-2H-indazoleHCID 117798677—

Reaction Steps

To a solution of 1-(3-bromo-2,6-difluorophenyl)ethanone (4.25 g) in n-butanol (50 ml) was added hydrazine monohydrate (1.06 ml) at room temperature, and the mixture was heated under reflux for 20 hr. The reaction mixture was cooled, and added to water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate). The residue was dissolved in ethyl acetate (50 ml), trimethyloxonium tetrafluoroborate (4.01 g) was added at room temperature, and the mixture was stirred at the same temperature for 3 hr. The reaction mixture was added dropwise to water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (224 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199963B2
Source datasetuspto-grants-2015_12
ORD IDord-a5794697f9c74ed0a84667773c2f6c72
Source noteuspto-grants-2015_12