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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2268227Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/2268227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
Edukt4-ChlorophenolHCID 4684—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt3-(4-Chlorophenoxy)propionic acidHCID 76780—
Edukt1H-Imidazole-1-propanamineHCID 78736—
Edukt3-Phenoxypropionic acidHCID 81596—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]propionamideHCID 18349808—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06326500B1
Quelldatensatzuspto-grants-2001_12
ORD IDord-ebe8e3f338d8429a85a24e10eb934ecf
Quellennotizuspto-grants-2001_12