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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182393Generated: November 1, 2026

Tetrafluoroboric acid → 4-Fluoro-1H-indazole

https://huagongshe.com/reaction/2182393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
Reactant3-Fluoro-2-methylanilineHCID 285553—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Fluoro-1H-indazoleHCID 22477757—

Reaction Conditions

Temperature0 °C

Reaction Steps

To tetrafluoroboric acid (8.2 ml, 48 wt % in water) was added 3-fluoro-2-methylaniline (2.27 ml). The mixture was cooled to 0° C. when a precipitate formed which was redissolved by the addition of water (8 ml). A solution of sodium nitrite (1.38 g) in water (2.7 ml) was then added dropwise and the mixture was then allowed to warm to ambient temperature and then stirred for a further 1 hour. The precipitated solid was filtered, then washed with diethyl ether, and then dried under suction for 30 minutes. The resulting tetrafluoroborate salt was added to a suspension of potassium acetate (3.92 g) and 18-crown-6 (0.264 g) in chloroform (45 ml). After stirring for 3 hours at ambient temperature the bright orange mixture was filtered and the insoluble material was washed with dichloromethane, then subjected to flash column chromatography on silica eluting with a mixture of 40/60 petrol and ethyl acetate (3:1 v/v) to give 4-fluoro-1H-indazole (0.675 g) as an off-white solid. LC-MS (METHOD B): RT=2.70 minutes; 137 (M+H)+. (c) 4-Chloro-1H-indazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-25ed861f790c4579b1c19ea2902035ea
Source noteuspto-grants-2005_05