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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412042Generated: October 28, 2026

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

https://huagongshe.com/reaction/412042

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-ethoxy-benzoic 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562830B1
Source datasetuspto-grants-2003_05
ORD IDord-e0608f1eacbe4d7a9d833a504386827c
Source noteuspto-grants-2003_05