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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859669Generated: November 1, 2026

3-Amino-4-methoxybenzanilide → HCID 18626281, compound

https://huagongshe.com/reaction/1859669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-4-methoxybenzanilideHCID 8426—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-3-nitrobenzeneHCID 12574—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventMesityleneHCID 7947—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 18626281HCID 186262816.2%

Reaction Steps

A mixture of 3-amino-4-methoxy-N-phenyl-benzamide (2.0 g, 8 mmol), 1-iodo-3-nitrobenzene (2.5 g, 10 mmol), potassium carbonate (2.8 g, 20 mmol), and copper(I) iodide (0.4 g, 2 mmol) in mesitylene (20 mL) was stirred under an inert atmosphere and heated to reflux. After 48 hours, the mixture was allowed to cool and was then diluted with tetrahydro-furan (100 mL) and filtered through Celite. The filtrate was stripped of solvent under reduced pressure to leave an oily residue which was dissolved in ethyl acetate (250 mL) and extracted successively with 2N hydrochloric acid (2×200 mL), water, 0.5 M aqueous potassium carbonate, water, and saturated aqueous sodium chloride, then dried over MgSO4. The solution was filtered and the filtrate stripped of solvent under reduced pressure. The resulting residue was subjected to chromatography on a column of silica gel in chloroform to afford the product (0.18 g); m.p. 220-221° C. after recrystallization from acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528528B2
Source datasetuspto-grants-2003_03
ORD IDord-a6732ebe5c5e4caaa90e643749134cf9
Source noteuspto-grants-2003_03