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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347632Generated: October 25, 2026

Hydrochloric Acid → 4-Bromo-2,6-dimethylbenzonitrile

https://huagongshe.com/reaction/347632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CyanideHCID 9032—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2,6-xylidineHCID 90549—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418260HCID 178418260—
SolventWaterHCID 962—
Product4-Bromo-2,6-dimethylbenzonitrileHCID 10910795—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromo-2,6dimethylaniline (4.49 g, 22.4 mmol) was taken up in water (25 ml) and concentrated hydrochloric acid (8.0 ml) was added. The mixture was sonicated to form a fine suspension and then cooled to 0° C. A solution of sodium nitrite (1.67 g, 24.2 mmol) in water (5 ml) was then added dropwise so as to maintain the temperature of the reaction between 0–5° C. The mixture was stirred at 0–5° C. for ½ h and then neutralised by addition of solid sodium carbonate. The resulting solution was then added portionwise to a solution of copper cyanide (2.42 g, 27.0 mmol) and potassium cyanide (3.65 g, 56.1 mmol) in water (25 ml) at 70° C. The mixture was stirred at 70° C. for ½ h, allowed to cool and then extracted with toluene (2 times). The combined extracts were washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography on silica (eluant EtOAc:pet. ether 5:95) to give an orange solid; yield 3.2 g (68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176195B2
Source datasetuspto-grants-2007_02
ORD IDord-f68d93a22edb4c43998a912d20a81b04
Source noteuspto-grants-2007_02