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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269790Generated: October 30, 2026

4-Nitrophenol → HCID 70214878, compound

https://huagongshe.com/reaction/2269790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 70215951HCID 70215951—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
ProductHCID 70214878HCID 70214878—

Reaction Steps

Into 20 ml of dichloromethane, 0.81 g (3.8 mmol) of (E) 3-(2-amino-4-chlorophenyl)-2-methyl-2-propenoic acid and 1.0 g of p-nitrophenol (manufactured by Wako Pure Chemical Industries, Ltd.) were dissolved; and 40 mg of dimethylaminopyridine (manufactured by Wako Pure Chemical Industries, Ltd.) were added thereto. Further, while the mixture was stirred under cooling with ice, 1.0 g of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC-HCl) (manufactured by Wako Pure Chemical Industries, Ltd.) was added thereto in portions. The mixture was returned to room temperature and then was stirred for 20 hours. After the end point of this reaction was verified by TLC, the reaction liquid was concentrated under a reduced pressure and then was dissolved in 100 ml of ethyl acetate. This solution was washed several times with a 5% aqueous sodium hydrogencarbon ate solution and then with a saturated aqueous sodium chloride solution, and was dried with magnesium sulfate anhydride. Thereafter, the solvent was evaporated, whereby a crude product was obtained. This product was recrystallized from ethanol, whereby 1.2 g of the aimed compound were obtained as a crystal (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329546B1
Source datasetuspto-grants-2001_12
ORD IDord-8085fb8b569d4193af7110ed4f638e17
Source noteuspto-grants-2001_12