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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654435Generated: October 30, 2026

Ethyl Acetate → HCID 14720869, compound

https://huagongshe.com/reaction/654435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant1H-Imidazole, 4,5-dichloro-1-(chloromethyl)-HCID 14402692—
Reactant4-[(3,6-Dimethyl-2-pyrazinyl)oxy]phenolHCID 19937608—
SolventDimethylformamideHCID 6228—
ProductHCID 14720869HCID 1472086967.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

At room temperature (about 20° C.), 7.8 g of 4-(3,6-dimethyl-2-pyrazinyloxy)-phenol in 20 ml of anhydrous dimethylformamide is dripped into 1.3 g of 80% strength sodium hydride in 30 ml of anhydrous dimethylformamide. The mixture is stirred for one hour at 70° C., and then 6.68 g of 1-chloromethyl-4,5-dichloroimidazole in 30 ml of anhydrous dimethylformamide is dripped in. The mixture is stirred for 8 hours at 70° C. and overnight at room temperature. It is then stirred into 200 ml of ethyl acetate, and this mixture is washed twice with water, four times with 5% strength sodium hydroxide solution and twice with saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and the solvent is evaporated off under reduced pressure. The crude product obtained is crystallized with n-hexane. There is obtained 8.9 g of 1-[4-(3,6-dimethyl-2-pyrazinyloxy)-phenoxymethyl]-4,5-dichloroimidazole; m.p.: 84°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132308
Source datasetuspto-grants-1992_07
ORD IDord-7d6b2d99b8b340bc917fec93306e9804
Source noteuspto-grants-1992_07