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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698744Generated: October 30, 2026

Ethyl Acetate → HCID 72312772, compound

https://huagongshe.com/reaction/1698744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N,N-dimethylacetamideHCID 75886—
ReactantHCID 72312790HCID 72312790—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 72312772HCID 72312772—

Reaction Steps

After adding 0.163 g of potassium carbonate and 0.14 ml of 2-chloro-N,N-dimethylacetamide to a solution of 0.41 g of {2-(5-ethyl-2-fluoro-3-hydroxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene}carbamic acid methyl ester in 15 ml of DMF, the reaction mixture was stirred at room temperature for 60 hours, and then 200 ml of ethyl acetate and 100 ml of water were added. The organic layer was washed twice with 100 ml of water and once with 100 ml of saturated aqueous sodium chloride in that order, and dried over anhydrous magnesium sulfate. The desiccating agent was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (0.41 g) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163787B2
Source datasetuspto-grants-2012_04
ORD IDord-4ed0f679313a4d5794e4de83c528356a
Source noteuspto-grants-2012_04