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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-Bromo-4-chloro-6-fluoroaniline | HCID 2736222 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-4-chloro-6-fluorobenzonitrile | HCID 58579537 | 38.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912221B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-67b4ba064f6a49da8dc617510ef2f2e6 |
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| Source note | uspto-grants-2014_12 |
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