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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271216Generated: October 26, 2026

Ethyl Acetate → N-acetyl-N-(2-methoxyphenyl)-2-phenoxyaniline

https://huagongshe.com/reaction/2271216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactanto-IodoanisoleHCID 68257—
Reactant2-PhenoxyacetanilideHCID 897080—
CatalystCopperHCID 23978—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventNitrobenzeneHCID 7416—
ProductN-acetyl-N-(2-methoxyphenyl)-2-phenoxyanilineHCID 18407187—

Reaction Steps

In 20 ml of nitrobenzene were refluxed 2.27 g of N-acetyl-2-phenoxyaniline, 1.3 ml of 2-iodoanisole, 1.38 g of potassium carbonate, 133 mg of a copper powder and 200 mg of copper bromide under heating for 8 hours. The reaction solution was cooled to room temperature, and after addition of ethyl acetate, the insoluble matter was removed by filtration. The filtrate was washed with 0.5 N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate-hexane=1:4) to give 660 mg of N-acetyl-N-(2-methoxyphenyl)-2-phenoxyaniline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333358B1
Source datasetuspto-grants-2001_12
ORD IDord-9990bf1717b7486d8b3798728ce3f9c8
Source noteuspto-grants-2001_12