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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261752Generated: November 2, 2026

Potassium Carbonate → 1-(4-Chloro-2-phenylaminophenyl)ethanone

https://huagongshe.com/reaction/1261752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
Reactant1-(2-Amino-4-chlorophenyl)ethanoneHCID 13574717—
CatalystCopperHCID 23978—
SolventButyl etherHCID 8909—
Product1-(4-Chloro-2-phenylaminophenyl)ethanoneHCID 5984617667.6%

Reaction Conditions

Temperature142.5 °C

Reaction Steps

A 3-necked round-bottomed flask equipped with a mechanic stirrer, a thermocouple probe, a reflux condenser and a nitrogen bubbler was charged with 1-(2-amino-4-chlorophenyl)ethanone (81 g, 478 mmol) in di-n-butyl ether (1 L). The reaction was then treated with pulverized potassium carbonate (200 g, 1.45 mol) and copper powder (5 g, 78 mmol). The reaction mixture was refluxed at 140-145° C. for 3 h. At this time, additional potassium carbonate (100 g, 0.72 mol), iodobenzene (100 g, 0.49 mol) and copper powder (2 g, 31 mmol) was added. The resulting mixture was refluxed overnight. At this time, the reaction was cooled to 25° C., filtered and washed with methyl tert-butyl ether. The filtrate was concentrated in vacuo. Flash chromatography (4″×16″ silica gel column; 0-2% ethyl acetate/hexanes) followed by concentration of the appropriate fractions, slurrying with hexanes, filtration and drying afforded 1-(4-chloro-2-phenylamino-phenyl)-ethanone (79.3 g, 67.6%) as a yellow solid. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471027B2
Source datasetuspto-grants-2013_06
ORD IDord-4ed766c874474fbebb0808cb7d630a30
Source noteuspto-grants-2013_06