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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956834Generated: October 26, 2026

Phenol → 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide

https://huagongshe.com/reaction/1956834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant4-ChlorophenolHCID 4684—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(4-Chlorophenoxy)propionic acidHCID 76780—
Reactant1H-Imidazole-1-propanamineHCID 78736—
Reactant3-Phenoxypropionic acidHCID 81596—
SolventTetrahydrofuranHCID 8028—
Product3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamideHCID 18349808—

Reaction Steps

A solution of 3-(4-chlorophenoxy)propionic acid (5.0 g, prepared from 4-chlorophenol by the process described in J.A.C.S. 1923, 2708 for the conversion of phenol into 3-phenoxypropionic acid) in THF (90 ml) was treated with 1,1'-carbonyldiimidazole (4.05 g) at room temperature with stirring. The mixture was stirred at ambient temperature for two hours. 1-(3-Aminopropyl)imidazole (3.12 g) was added and the mixture was stirred at ambient temperature for 18 hours. The solvent was distilled off and the residue was dissolved in dichloromethane, washed with water, dried and then evaporated to give a solid which was recrystallised from ethyl acetate to give 3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamide, m.p. 114°-115.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780642
Source datasetuspto-grants-1998_07
ORD IDord-12330c4a033a4ed0a914490f75aff133
Source noteuspto-grants-1998_07