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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283701Generated: October 31, 2026

Triethyloxonium tetrafluoroborate → HCID 90308796, compound

https://huagongshe.com/reaction/2283701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant5-Bromo-7-chloro-1H-indazoleHCID 21102194—
SolventEthyl AcetateHCID 8857—
ProductHCID 90308796HCID 90308796—

Reaction Steps

Triethyl oxonium tetrafluoroborate (2.5 g) was added to a solution of 5-bromo-7-chloro-1H-indazole (1.38 g) in ethyl acetate (15 mL), and the reaction solution was stirred at room temperature overnight. After dilution with ethyl acetate, the reaction solution was washed successively with water and a saturated saline solution, dried over anhydrous sodium sulfate, and the solvent was evaporated under vacuum. The resultant residue was purified by column chromatography on silica gel (developing solvent:hexane/ethyl acetate) to obtain 5-bromo-7-chloro-2-ethyl-2H-indazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145414B2
Source datasetuspto-grants-2015_09
ORD IDord-cc88bc3fb81546f183935a56e3238cf5
Source noteuspto-grants-2015_09