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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268253Generated: October 30, 2026

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

https://huagongshe.com/reaction/2268253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodium hydrideHCID 24758—
Reactant2-[3-(Imidazol-1-yl)propylamino]-2-methyl-1-propanolHCID 18349765—
SolventDimethylacetamideHCID 31374—
ProductN-[2-(4-chlorobenzyloxy)-1,1-dimethylethyl]-3-(imidazol-1-yl)propylamineHCID 18349726—

Reaction Conditions

Temperature30 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326500B1
Source datasetuspto-grants-2001_12
ORD IDord-4a0ff415b89949c7861f7f36b99955e0
Source noteuspto-grants-2001_12