HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288357Generated: October 26, 2026
Triethylamine → 4-Methylamino-3-nitro-benzoic acid-n-phenyl-n-(2-ethoxy-carbonylethyl)-amide
https://huagongshe.com/reaction/2288357
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Methylamino)-3-nitrobenzoyl chloride | HCID 17946449 | — |
| Reactant | N-(2-ethoxy-carbonylethyl)aniline | HCID 86755521 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methylamino-3-nitro-benzoic acid-n-phenyl-n-(2-ethoxy-carbonylethyl)-amide | HCID 88183807 | — |
Reaction Steps
To a solution of 24.7 g (0.115 mol) of 4-methylamino-3-nitro-benzoic acid chloride and 22.3 g (0.115 mol) of N-(2-ethoxy-carbonylethyl)-aniline in 300 ml of tetrahydrofuran, 13.1 g (0.13 mol) of triethylamine were added dropwise in 15 minutes, with stirring, at room temperature. After 2 hours stirring the solvent was distilled off in a water-jet vacuum and the residue was mixed with 700 ml of water with stirring. The mixture was extracted 3 times with 200 ml of dichloromethane, the organic extract was washed twice with 200 ml of 2N hydrochloric acid and twice with 300 ml of water and dried over sodium sulphate. The solvent was then distilled off and the oily product thus obtained was purified by column chromatography (1 kg silica gel; eluant: petroleum ether/ethyl acetate=2:1). Yield: 35.0 g (82% of theory), Rf value: 0.28 (silica gel; dichloromethane/ethanol=50:1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06087380 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-1d41ed5a7eb44b95874c96566f77b567 |
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| Source note | uspto-grants-2000_07 |
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