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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491517Generated: November 1, 2026

Potassium Carbonate → Ethyl 1-(2-acetoxyethyl)-6-(2,3-dichlorobenzyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/491517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 6-(2,3-dichlorobenzyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 23083968—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(2-acetoxyethyl)-6-(2,3-dichlorobenzyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 2308394595%

Reaction Conditions

Temperature80 °C

Reaction Steps

Ethyl 6-(2,3-dichlorobenzyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylate (400 mg, 1.1 mmol) obtained in Step 3 was suspended in dimethylformamide (DMF; 8 ml), 2-bromoethyl acetate (152 μl, 1.4 mmol) and potassium carbonate (440 mg, 3.2 mmol) were added, and the mixture was stirred with heating at 80° C. 2-Bromoethyl acetate (152 μl, 1.4 mmol) was added twice on the way, and the mixture was stirred with heating at 80° C. for 1.5 hr in total. After allowing to cool, saturated aqueous ammonium chloride was added to the reaction mixture, and the precipitated solid was collected by filtration, washed with water, and vacuum dried to give the object product (468 mg, yield 95%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531554B2
Source datasetuspto-grants-2009_05
ORD IDord-4915396e966b4f0bb34f8fe36b0da60d
Source noteuspto-grants-2009_05