Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004350Generated: October 31, 2026

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

https://huagongshe.com/reaction/1004350

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

N,N-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 numberUS06048885
Source datasetuspto-grants-2000_04
ORD IDord-785c0615a7a74c07ac56c59a0da49aab
Source noteuspto-grants-2000_04