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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17736Generated: October 26, 2026

Ethyl Acetate → 4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/17736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-ethylphenolHCID 84223—
SolventDimethylformamideHCID 6228—
Product4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 66977523—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 4-chloro-3-ethylphenol (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was poured into EtOAc (100 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(4-chloro-3-ethylphenoxy)-1-nitrobenzene. The crude product was used for further transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737285B2
Source datasetuspto-grants-2010_06
ORD IDord-c9b591b7bdb2490a88e07295fec5b175
Source noteuspto-grants-2010_06