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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888251Generated: November 1, 2026

1-Methylnaphthalene → 2-Amino-5-cyano-N,3-dimethylbenzamide

https://huagongshe.com/reaction/888251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylnaphthaleneHCID 7002—
ReactantSodium CyanideHCID 8929—
Reactant2-amino-5-bromo-N,3-dimethylbenzamideHCID 44227575—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
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 100-mL, three-necked flask equipped with a mechanical stirrer, thermometer and condenser was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (5.0 g, 0.020 mol, 99.1% purity) and 1-methylnaphthalene (20 g) while maintaining a flow of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature, and powdered sodium cyanide (powdered just prior to use) (1.25 g, 0.024 mol, assuming 95% purity), copper(I) iodide (0.57 g, 0.0030 mol) and 4-(dimethylamino)pyridine (2.10 g, 0.017 mol) were added. The mixture was heated at 160 to 165° C. for 4.25 h and then allowed to cool to 25° C. Water (20 mL) was added dropwise to the reaction mixture over 5 minutes while stirring. After stirring for an additional 30 minutes, the reaction mixture was filtered, and the solid collected was washed with water (3×10 mL) and xylenes (10 mL), and then dried to a constant weight in a vacuum-oven at 50° C. to give the title compound as a light brown solid (3.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247570B2
Source datasetuspto-grants-2012_08
ORD IDord-812ba1dd127a4bbca14c717f9941bcc1
Source noteuspto-grants-2012_08