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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1363418Erstellt: 26. Oktober 2026

Sodium Cyanide → 2-Bromo-4-nitrobenzonitrile

https://huagongshe.com/reaction/1363418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CyanideHCID 8929—
EduktNitrous AcidHCID 24529—
EduktBenzenamine, 2-bromo-4-nitro-HCID 25840—
EduktSodium BicarbonateHCID 516892—
EduktSodium NitriteHCID 23668193—
EduktHCID 178418546HCID 178418546—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt2-Bromo-4-nitrobenzonitrileHCID 22351298—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Compound of example 168 (20 g, 92.2 mmol) was dissolved in 10% aqueous H2SO4 (100 mL) and the solution was cooled to 0° C. A solution of NaNO2 (7.64 g, 110 mmol) in water (20 mL) was added dropwise maintaining the temperature between 0-5° C. The mixture was stirred for 10 min., excess nitrous acid was neutralized using a saturated aqueous NaHCO3 solution. The resulting mixture was then added to a precooled (0-5° C.) suspension of CuCN (9.46 g, 105 mmol) and NaCN (5.20 g, 106 mmol) in water (200 mL). It was stirred for 10 min., and allowed to attain room temperature. It was stirred for 0.5 h and finally heated on a steam bath for 0.5 h. Excess saturated FeCl3 solution was then added to the reaction mixture. It was extracted using EtOAc (3×200 mL). The organic extract was washed with water, dried (anhydrous Na2SO4), concentrated and purified using a silica gel column and CHCl3 petroleum ether (60-80° C.) (1:1) as eluant to obtain the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07884127B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-ccce59bbe44f43ed8cc35db43b3a9691
Quellennotizuspto-grants-2011_02