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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Amino-3-methylbenzamide | HCID 14221807 | — |
| Reactant | 5-Acetyl-2-ethoxybenzoic acid | HCID 18536588 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Acetyl-ethoxybenzamido)-3-methylbenzamide | HCID 18536582 | 436.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482941 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-2e1cfb9d4f74440199ae167b5fa618c9 |
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| Source note | uspto-grants-1996_01 |
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