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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378597Generated: October 25, 2026

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

https://huagongshe.com/reaction/378597

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 numberUS06031109
Source datasetuspto-grants-2000_02
ORD IDord-133c6d49555047b9ace0b93851c7481d
Source noteuspto-grants-2000_02