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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079314Generated: November 2, 2026

2-Amino-4-methylbenzonitrile → N-(2-cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamide

https://huagongshe.com/reaction/2079314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylbenzonitrileHCID 2801276—
Reactant2-Methoxy-6-methylbenzoyl chlorideHCID 12892675—
SolventPyridineHCID 1049—
ProductN-(2-cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamideHCID 5801093277.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-4-methyl-benzonitrile (15.4 g, 0.117 mol) was dissolved in 100 mL pyridine and cooled to 0° C. To this mixture was added dropwise 2-methoxy-6-methylbenzoyl chloride (24 g, 0.13 mol, 1.1 equiv). During the addition the temperature did not exceed 2° C. The reaction was stirred at room temperature for 48 hours. The mixture was poured into 400 mL ice water, and the precipitate was collected by filtration and washed with water. The crude product was dissolved in 600 mL CH2Cl2, and the solution was washed twice with 500 mL of a 1 N HCl solution and once with 400 mL of a saturated aq. NaCl solution. The CH2Cl2 layer was dried over Na2SO4, filtered, and concentrated to dryness to yield 25.44 g (0.09 mol, 77.6%) of N-(2-cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-5fecdee2b13b41bba482ecf94abbe377
Source noteuspto-grants-2011_04