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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238954Generated: October 31, 2026

Ethyl Acetate → HCID 67359723, compound

https://huagongshe.com/reaction/238954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-2-fluoro-1-nitrobenzeneHCID 69691—
SolventDimethylformamideHCID 6228—
ProductHCID 67359723HCID 67359723—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-chloro-2-fluoronitrobenzene (3.0 g, 17.0 mmol) in DMF (8.7 mL), 4-fluorophenol (2.0 g, 17.9 mmol) and potassium carbonate (2.46 g, 17.9 mmol) were successively added, and the mixture was stirred at 70° C. for 2 hours. After the reaction, the mixture was cooled to room temperature and ethyl acetate was added to the mixture. After the organic phase was washed with water (30 mL), 1N sodium hydroxide (aq., 30 mL) and saturated brine (20 mL), it was dried with sodium sulfate. The solvent was distilled off under reduced pressure to give 4-chloro-2-(4-fluorophenoxy)-1-nitrobenzene as a crude product. The obtained compound was used for the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642640B2
Source datasetuspto-grants-2014_02
ORD IDord-29e8740d03c3456f902ba2766877a85f
Source noteuspto-grants-2014_02