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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323965Erstellt: 25. Oktober 2026

Toluene → N-[2-(4-chlorobenzyloxy)-1,1-dimethylethyl]-3-(imidazol-1-yl)propylamine

https://huagongshe.com/reaction/323965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
EduktSodium hydrideHCID 24758—
Edukt2-[3-(Imidazol-1-yl)propylamino]-2-methyl-1-propanolHCID 18349765—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-[2-(4-chlorobenzyloxy)-1,1-dimethylethyl]-3-(imidazol-1-yl)propylamineHCID 18349726—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

A solution of 2-[3-(imidazol-1-yl)propylamino]-2-methyl-1-propanol (1.5 g) in dimethyl acetamide (10 ml) was added dropwise to a stirred suspension of sodium hydride (0.32 g of a 60% dispersion in mineral oil) in dimethyl acetamide (15 ml) at 30° C. under nitrogen. The mixture was stirred for 45 minutes at 30° C. and then a solution of 4-chlorobenzyl chloride (1.63 g) in dimethyl acetamide (5 ml) was added. After the addition, the mixture was heated at 100-105° C. for 30 minutes and then cooled to 25° C. Toluene (50 ml) was added and the mixture was washed with water. The toluene layer was extracted with 5M hydrochloric acid. The combined acid extracts were basified with concentrated sodium hydroxide solution with cooling and extracted with dichloromethane to give an oil which was distilled under high vacuum to give N-[2-(4-chlorobenzyloxy)-1,1-dimethylethyl]-3-(imidazol-1-yl)propylamine, b.p. 180-185° C. at 0.3 mbar.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06215001B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-f13bd58339324978a6c842ef6a00ce81
Quellennotizuspto-grants-2001_04