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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551973Generated: October 26, 2026

4-Iodoaniline → 4-(4-Butylphenylethynyl)phenylamine

https://huagongshe.com/reaction/551973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanilineHCID 10893—
Reactant1-Butyl-4-ethynylbenzeneHCID 2775132—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-(4-Butylphenylethynyl)phenylamineHCID 5755450948.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-iodoaniline (20 g, 91 mmol, Aldrich) and 1-eth-1-ynyl-4-butylbenzene (16.7 g, 105 mmol, Aldrich) in dry acetonitrile (300 mL) under nitrogen was added CuI (0.83 g, 4.3 mmol), TEA (27.7 g, 273 mmol) followed by Pd(PPh3)2Cl2 (3 g, 4.3 mmol). The reaction mixture was stirred at 85° C. for 24 hours and the solvent was removed under reduced pressure. The residue was diluted with Et2O (200 mL) and washed with water, brine and dried (MgSO4). The solvent was removed under reduced pressure and the crude product was purified by chromatography (Pet Ether/EtOAc (4/1) to give 11 g (47%) of the title compound as a solid. TLC-Pet ether/EtOAc (4/1): Rf=0.35. HPLC purity >98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947851B2
Source datasetuspto-grants-2011_05
ORD IDord-fe1046cc64df492b9b37fca70bdc3a8d
Source noteuspto-grants-2011_05