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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489383Generated: November 2, 2026

Imidazole → 2-(2,4-dichlorobenzyloxy)-alpha-(1-imidazolyl)benzaldehyde O-methyloxime

https://huagongshe.com/reaction/1489383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
Reactantalpha-chloro-2-(2,4-dichlorobenzyloxy)benzaldehyde O-methyloximeHCID 53754588—
SolventDimethylformamideHCID 6228—
Product2-(2,4-dichlorobenzyloxy)-alpha-(1-imidazolyl)benzaldehyde O-methyloximeHCID 5421294348.5%

Reaction Steps

Imidazole (2.04 g) was dissolved in DMF (30 ml), and 60% sodium hydride (1.20 g) was added. The mixture was stirred at room temperature for 10 minutes, then α-chloro-2-(2,4-dichlorobenzyloxy)benzaldehyde O-methyloxime (5.17 g) was added, and the mixture was stirred at 120° C. for 2 hours. After completion of the reaction, ether (200 ml) was added, and the mixture was washed with brine (200 ml) twice, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography and recrystallized from ethyl acetate/n-hexane to give 2-(2,4-dichlorobenzyloxy)-α-(1-imidazolyl)benzaldehyde O-methyloxime (2.74 g) as colorless crystals. mp. 122°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677465
Source datasetuspto-grants-1997_10
ORD IDord-1d27698525d348df9e7f139190ce8563
Source noteuspto-grants-1997_10