Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978039Generated: October 26, 2026

Dimethylformamide → 4-Chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazole

https://huagongshe.com/reaction/978039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Ethoxyphenoxy)benzyl chlorideHCID 13730380—
ReactantHCID 178432150HCID 178432150—
SolventWaterHCID 962—
Product4-Chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazoleHCID 1373038134.1%

Reaction Steps

To a mixture of anhydrous N,N-dimethylforamide (10 ml) and sodium hydride (62% oil suspension; 0.071 g), 4-chloro-2-methylbenzimidazole (0.304 g) was added while stirring, and the stirring was continued at room temperature for 1 hour. The resultant mixture was cooled to 5°-10° C., and a solution of 4-(4-ethoxyphenoxy)benzyl chloride (0.400 g) in anhydrous N,N-dimethylformaide (10 ml) was dropwise added thereto in 30 minutes, followed by stirring at room temperature overnight. After completion of the reaction, the reaction mixture was poured into water (100 ml) and extracted with toluene (30 ml) two times. The toluene extract was washed with water, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove toluene. The residue was purified by silica gel column chromatography to give 4-chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazole (0.204 g) as a colorless liquid. nD26.5 1.6087.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663339
Source datasetuspto-grants-1987_05
ORD IDord-c19943473bb44129a190c8b13b394e5d
Source noteuspto-grants-1987_05