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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279443Generated: October 30, 2026

Imidazole → 1-[2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl]imidazole

https://huagongshe.com/reaction/279443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl chlorideHCID 54432646—
SolventDiethyl EtherHCID 3283—
Product1-[2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl]imidazoleHCID 5399543765.3%

Reaction Steps

Dimethylformamide (3 ml) and 60% sodium hydride (0.16 g, 3.9 mmol) were added to imidazole (0.27 g, 3.9 mmol), and the mixture was stirred at room temperature for 10 minutes. Then, 2-(3-chlorophenoxymethyl)-α-methoxyiminobenzyl chloride (0.40 g, 1.3 mmol) was added, and the mixture was stirred at 110° C. for 2 hours. After completion of the reaction, ether (100 ml) was added, and the mixture was washed with brine (80 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 1-[2-(3-chlorophenoxymethyl)-α-methoxyiminobenzyl]imidazole (0.29 g, 65.3%) as colorless crystals. mp. 96.5-97.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-83aa2cd0f955485f870949d6486719a2
Source noteuspto-grants-2002_03