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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242233Generated: October 29, 2026

Potassium Carbonate → N,N-dimethyl-5-methyl-2-(2',4'-dichloro-6'-methylanilino)phenylacetamide

https://huagongshe.com/reaction/1242233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Dichloro-6-methylanilineHCID 1268287—
ReactantN,N-dimethyl-5-methyl-2-iodophenylacetamideHCID 15541938—
CatalystCopperHCID 23978—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductN,N-dimethyl-5-methyl-2-(2',4'-dichloro-6'-methylanilino)phenylacetamideHCID 15541937—

Reaction Steps

N,N-Dimethyl-5-methyl-2-iodophenylacetamide (3.5 g, 11.5 mmol) and 2,4-dichloro-6-methylaniline (4.1 g, 23 mmol) are stirred in xylenes (100 ml) with copper powder (0.18 g, 2.9 mmol), copper(I) iodide (0.55 g, 2.9 mmol) and anhydrous potassium carbonate (1.6 g, 11.5 mmol). The reaction is heated to reflux temperature for 48 hours. While still slightly warm (40°) the brown suspension is filtered through a pad of Celite, which in turn is rinsed with toluene (75 ml). The filtrate is evaporated on a rotovap and flash chromatographed on silica gel (Rf 0.30 in 40% EtOAc/hexane) to give N,N-dimethyl-5-methyl-2-(2′,4′-dichloro-6′-methylanilino)phenylacetamide as an off-white crystalline solid, m.p. 119–124°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115662B2
Source datasetuspto-grants-2006_10
ORD IDord-a21189c863074e8aab8864203ab50935
Source noteuspto-grants-2006_10