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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514821Generated: October 29, 2026

3-Aminoquinoline → 3-Fluoroquinoline

https://huagongshe.com/reaction/514821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminoquinolineHCID 11375—
ReactantTetrafluoroboric acidHCID 28118—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-FluoroquinolineHCID 96405—

Reaction Steps

Quinolin-3-amine (4 g, 27.7 mmol) was added to HBF4 (26 mL, 48% aqueous solution) portionwise at room temperature, and the mixture was stirred at room temperature until it became homogeneous. The mixture was then cooled to 0° C., and a solution of NaNO2 (2.4 g, 34.8 mmol) in H2O (8 mL) was added dropwise, when the reaction mixture became heterogeneous. The mixture was stirred at 0° C. for 1 hour, then the mixture was filtered, and the filtered cake was washed with cold EtOH, then Et2O. The resulting solid was dried under vacuum, then suspended in toluene in a round bottom flask and was refluxed for 1.5 hours. The resulting mixture was cooled to room temperature, and then poured into cold water. The organic layer was dried over Na2SO4, and then concentrated in vacuo to obtain the desired product (1.6 g). LC-MS: m/z 148.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-28ac9751e0624fa4b5b21bb1223fcf4c
Source noteuspto-grants-2015_08