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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887782Generated: October 30, 2026

Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) → methyl 5-bromo-6-fluoro-2-methyl-2H-indazole-4-carboxylate

https://huagongshe.com/reaction/887782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
ReactantMethyl 5-bromo-6-fluoro-1H-indazole-4-carboxylateHCID 59145874—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Productmethyl 5-bromo-6-fluoro-2-methyl-2H-indazole-4-carboxylateHCID 5914584578%

Reaction Steps

To a solution of methyl 5-bromo-6-fluoro-1H-indazole-4-carboxylate (700 mg, 2.56 mmol) in ethyl acetate (26 mL) was added trimethyloxonium tetrafluoroborate (569 mg, 3.85 mmol) at room temperature, and the mixture was stirred for 2.5 hr. The reaction solution was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→50/50) to give the title compound (570 mg, yield 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-7fddd5c934924e0f83d9aff864c9eec4
Source noteuspto-grants-2012_08