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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230495Generated: October 30, 2026

Dimethylformamide → 2-chloro-1-(2-ethoxyethyl)-1H-benzimidazole

https://huagongshe.com/reaction/2230495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthane, 1-chloro-2-ethoxy-HCID 12341—
ReactantSodium hydrideHCID 24758—
Reactant2-ChlorobenzimidazoleHCID 78572—
SolventEthyl AcetateHCID 8857—
SolventEthyl acetate hexaneHCID 21226206—
Product2-chloro-1-(2-ethoxyethyl)-1H-benzimidazoleHCID 10489356—

Reaction Conditions

Temperature60 °C

Reaction Steps

Combine 2-chloro-1H-benzimidazole (21.1.4 g, 138.4 mmol) and dimethylformamide (200 mL). Add portionwise, sodium hydride (24.0 g, 60% in oil, 153.3 mmol). After 15 minutes, add 2-chloroethyl ethyl ether (21.9 g, 201,5 mmol). Heat to 60° C. After 18 hours, cool the reaction mixture and dilute with ethyl acetate. Extract with a saturated aqueous sodium bicarbonate solution, water, and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% ethyl acetate/hexane and then 30% ethyl acetate hexane to give the 2-chloro-1-(2-ethoxyethyl)-1H-benzimidazole: Rf=0.74 (silica gel, 7/3 ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-8db30d83c3ab49b7bd4cb42644425222
Source noteuspto-grants-2002_07