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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288511Generated: October 28, 2026

4-Nitrobenzoic Acid → 4-Nitrobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

https://huagongshe.com/reaction/2288511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoic AcidHCID 6108—
ReactantTriethylamineHCID 8471—
ReactantN-Phenyl-beta-alanine methyl esterHCID 89103—
ReactantDichloromethane methanolHCID 21226129—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
Product4-Nitrobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amideHCID 18412341—

Reaction Steps

16.7 g (0.1 mol) of 4-nitrobenzoic acid were refluxed in 50 ml of thionyl chloride and 3 drops of dimethylformamide for 1 hour. After the solvent had been distilled off in vacuo the crude product was dissolved in 150 ml of tetrahydrofuran and added dropwise to a solution of 18 g (0.1 mol) of N-(2-methoxycarbonylethyl)aniline in 250 ml of tetrahydrofuran and 42 ml 0.3 mol) of triethylamine. After being stirred for one hour at ambient temperature the reaction mixture was diluted with 250 ml of ethyl acetate and washed 2× with 200 ml of 14% saline solution. After the solvent had been distilled off and the residue chromatographed (silica gel; methylene chloride) a yellow oil was obtained which slowly solidified. Yield: 32.6 g (100% of theory), Rf value: 0.37 (silica gel; methylene chloride/methanol=50:1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087380
Source datasetuspto-grants-2000_07
ORD IDord-7638b6de40bb4e3a943e3f1e9a99cb9e
Source noteuspto-grants-2000_07