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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404557Generated: October 26, 2026

Potassium Cyanide → 2-Bromo-4-chloro-6-fluorobenzonitrile

https://huagongshe.com/reaction/1404557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant2-Bromo-4-chloro-6-fluoroanilineHCID 2736222—
ReactantNitrilooxonium tetrafluoroborateHCID 11137142—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-chloro-6-fluorobenzonitrileHCID 5857953738.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 2-bromo-4-chloro-6-fluoro-phenylamine (10 g, 44.5 mmol) in anhydrous DCM (100 ml) was added nitrosonium tetrafluoroborate (5.72 g, 49.01 mmol) and the mixture was stirred at 25° C. for 1 h. The reaction mixture was then cooled to 0° C. prior to addition of KCN (5.8 g, 89.1 mmol) followed by a dropwise addition of an aqueous solution (50 ml) of cupric sulfate hexahydrate (22.24 g, 89.1 mmol). After stirring for 40 minutes at 0° C. the reaction mixture was allowed to warm to 25° C. and stirring was continued for 1 h. The reaction mixture was diluted with DCM (100 ml) and slowly quenched by the addition of aqueous saturated solution of NaHCO3 until gas evolution is no longer observed. The resulting heterogeneous mixture was then filtered through a pad of celite and the organic layer was separated, washed twice with brine, dried with Na2SO4 and evaporated. The crude residue thus obtained was purified by chromatography (silica gel; hexane/EtOAc 90:10) to obtain the title compound as reddish solid (4 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912221B2
Source datasetuspto-grants-2014_12
ORD IDord-67b4ba064f6a49da8dc617510ef2f2e6
Source noteuspto-grants-2014_12