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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374787Generated: October 25, 2026

Dimethylformamide → 2-(5-Acetyl-ethoxybenzamido)-3-methylbenzamide

https://huagongshe.com/reaction/374787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Amino-3-methylbenzamideHCID 14221807—
Reactant5-Acetyl-2-ethoxybenzoic acidHCID 18536588—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2-(5-Acetyl-ethoxybenzamido)-3-methylbenzamideHCID 18536582436.6%

Reaction Steps

Oxalyl chloride (3.66 g, 0.0288 mol) was added dropwise to a stirred solution of 5-acetyl-2-ethoxybenzoic acid (3 g, 0.00144 mol) and dimethylformamide (0.1 ml) in dichloromethane (15 ml). The mixture was stirred at room temperature for 3 hours, then the solvent evaporated under vacuum and the residue azeotroped with hexane (3×50 ml). The crude acyl chloride was dissolved in dichloromethane (20 ml) and the solution added dropwise to a stirred solution of 2-amino-3-methylbenzamide (2.16 g, 0.0144 mol) in pyridine (40 ml) at 0° C. The mixture was allowed to warm to room temperature and stirred for a further 18 hours. The solvent was removed by evaporation under vacuum, the residue dissolved in dichloromethane (50 ml) and this solution then washed with saturated aqueous sodium carbonate solution (50 ml), 2N hydrochloric acid (50 ml) and brine (50 ml), then dried (Na2SO4) and evaporated under vacuum. Trituration of the residue with diethyl ether gave the title compound as a white solid (2.14 g, 44%), m.p. 214°-216° C. Found: C,66.81; H,5.98; N,8.16. C19H20N2O4 requires C,67.04; H,5.92; N,8.23%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482941
Source datasetuspto-grants-1996_01
ORD IDord-2e1cfb9d4f74440199ae167b5fa618c9
Source noteuspto-grants-1996_01