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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885657Generated: October 25, 2026

Mesitylene → 2-Amino-5-cyano-N,3-dimethylbenzamide

https://huagongshe.com/reaction/885657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMesityleneHCID 7947—
ReactantSodium CyanideHCID 8929—
ReactantButylimidazoleHCID 61347—
Reactant2-amino-5-bromo-N,3-dimethylbenzamideHCID 44227575—
ReactantNaOH NaClOHCID 86647248—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
Product2-Amino-5-cyano-N,3-dimethylbenzamideHCID 25157282—

Reaction Steps

A 500-mL four-necked flask equipped with a mechanical stirrer, thermocouple, condenser, side-arm addition funnel and sodium hydroxide/sodium hypochlorite scrubber was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (24.6 g, 0.10 mol, 99% purity) and mesitylene (100 g) while maintaining an atmosphere of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature, and granular sodium cyanide (Alfa Aesar®, 7.7 g, 0.15 mol, assuming 95% purity), copper(I) iodide (2.9 g, 0.015 mol, 98% purity) and 1-butyl-1H-imidazole (10.8 g, 0.085 mol, 98% purity) were added to the reaction mixture, after which time the nitrogen inlet line was attached directly to the reaction flask. The reaction mixture was heated at reflux (about 166-170° C.) for 6 h, while venting through the scrubber and then allow to cool overnight. Water (100 mL) was added to the reaction mixture and stirring was continued for 45 minutes. More water (25 mL) was added to the reaction mixture and stirring continued for an additional 15 minutes. The mixture was filtered, and the solid collected was washed with water (3×50 mL), mesitylene (50 g) and dried to a constant weight in a vacuum-oven at 55° C. to give the title compound as a light yellow solid (16.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242279B2
Source datasetuspto-grants-2012_08
ORD IDord-d5959d86d1fa4de9b1fe48d2c137aae7
Source noteuspto-grants-2012_08