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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1034108Erstellt: 26. Oktober 2026

Potassium Cyanide → 2,6-Difluoro-4-iodobenzonitrile

https://huagongshe.com/reaction/1034108

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CyanideHCID 9032—
EduktSodium HydroxideHCID 14798—
Edukt2,6-Difluoro-4-iodoanilineHCID 278943—
EduktSodium BicarbonateHCID 516892—
EduktSodium NitriteHCID 23668193—
KatalysatorCopper sulfate pentahydrateHCID 24463—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt2,6-Difluoro-4-iodobenzonitrileHCID 19023068—

Reaktionsschritte

12 g of sodium nitrite was dissolved in 91 ml of sulfuric acid and cooled to 10° C or less, and then 100 ml of acetic acid was added. At 20 to 25° C, 39 g of the 2,6-difluoro-4-iodoaniline from Step 3 was added to the solution, and then the solution was agitated for one hour. A second solution was made by dissolving 37 g of copper sulfate pentahydrate in 91 ml of water to which was added 62 g of ice, and this solution was added to the first. A third solution containing 39 of potassium cyanide dissolved in 92 ml of water, 221 g of sodium bicarbonate, and 91 ml of benzene was added to the first solution, and a diazonium salt sulfuric acid solution was added therein. After agitation at room temperature for 3 hours, a sodium hydroxide aqueous solution was added to dissolve the crystals. After being extracted with chloroform, the crystals were washed three times alternating with a 10% sodium hydroxide solution and water. After distillation of the chloroform, the residue was extracted with hexane, and the hexane was distilled off. This residue was recrystallized with methanol to obtain 6.7 g of 1,3-difluoro-2-cyano-5-iodobenzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05314640
Quelldatensatzuspto-grants-1994_05
ORD IDord-cd3685bbd7bf4494a31e80b65999d87a
Quellennotizuspto-grants-1994_05