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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427485Generated: November 1, 2026

Sodium Cyanide → 4-Bromo-2,6-dimethylbenzonitrile

https://huagongshe.com/reaction/2427485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2,6-xylidineHCID 90549—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418260HCID 178418260—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-Bromo-2,6-dimethylbenzonitrileHCID 1091079561.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromo-2,6-dimethylphenylamine (10 g, 500 mmol) was suspended in concentrated HCl (10 mL) and crushed ice (41 g) and cooled to 0° C. NaNO2 (3.52 g, 51 mmol) in water (10 mL) was added, maintaining a temperature of 0° C. and the reaction was stirred for 30 minutes. A solution of copper cyanide (5.60 g, 62.5 mmol) in water (25 mL) and sodium cyanide (7.79 g, 159 mmol) in water (12 mL) were cooled to 0° C. in a separate flask. The concentrated HCl mixture was neutralized with sodium carbonate and the resulting diazonium salt mixture was added to the copper cyanide and sodium cyanide solution along with toluene (100 mL) under vigorous stirring, maintaining a temperature of 0° C. for 1 hour, followed by stirring at room temperature for 4 hours. The reaction mixture was heated to 50° C. and then cooled to room temperature. The reaction was partitioned between water and toluene and the organic layers were combined and washed with water and dried over anhydrous Na2SO4. The product was purified by column chromatography on silica (20% EtOAc/Hexanes) to afford a brown solid (8.10 g). 1H NMR (300 MHz, CDCl3): δ 7.33 (s, 2H), 2.53 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-bce9b9b1e65f42b29ed4c8253f1479b8
Source noteuspto-grants-2011_06