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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378626Generated: October 25, 2026

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

https://huagongshe.com/reaction/378626

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 addled 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 numberUS06031109
Source datasetuspto-grants-2000_02
ORD IDord-94237408e91148f3a77e6fafe5bf8d62
Source noteuspto-grants-2000_02