Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646492Generated: November 1, 2026

Ethyl Acetate → HCID 14720869, compound

https://huagongshe.com/reaction/1646492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant1H-Imidazole, 4,5-dichloro-1-(chloromethyl)-HCID 14402692—
Reactant4-(3,6-Dimethyl-2-pyrazinyloxy)-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 numberUS05180727
Source datasetuspto-grants-1993_01
ORD IDord-4b8b4016966f4b0bafcbabb3621ee304
Source noteuspto-grants-1993_01