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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Methylamino)-3-nitrobenzoyl chlorideHCID 17946449—
ReactantN-(2-ethoxy-carbonylethyl)anilineHCID 86755521—
SolventTetrahydrofuranHCID 8028—
Product4-Methylamino-3-nitro-benzoic acid-n-phenyl-n-(2-ethoxy-carbonylethyl)-amideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087380
Source datasetuspto-grants-2000_07
ORD IDord-1d41ed5a7eb44b95874c96566f77b567
Source noteuspto-grants-2000_07