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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330842Generated: October 27, 2026

1-Ethynyl-4-methoxybenzene → N-Ethyl-2-[4-(4-methoxy-phenylethynyl)-phenyl]-propionamide

https://huagongshe.com/reaction/330842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-4-methoxybenzeneHCID 251020—
ReactantN-Ethyl-2-(4-iodo-phenyl)-propionamideHCID 66693450—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductN-Ethyl-2-[4-(4-methoxy-phenylethynyl)-phenyl]-propionamideHCID 56929774—

Reaction Steps

300 mg (0.99 mmol) N-Ethyl-2-(4-iodo-phenyl)-propionamide (XVIII.1) are added to 148 μL (1.14 mmol) 1-ethynyl-4-methoxybenzene in 8 mL ACN under inert gas atmosphere. 276 μL (1.99 mmol) TEA as base, 6 mg (0.03 mmol) copper(I)iodide and 42 mg (0.060 mmol) bis(triphenylphosphine)palladium(II)chloride as catalyst are added and the mixture is stirred at rt under inert gas atmosphere for 5 h. After that time, the mixture is diluted with EtOAc, washed with saturated ammonium chloride solution and brine, and the organic layer is dried over sodium sulphate. The solvent is evaporated and the residue is purified by column chromatography (silicia gel; heptane:EtOAc 50:50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877754B2
Source datasetuspto-grants-2014_11
ORD IDord-1dc9197ce3d74b39bd9f65ad4711d3f5
Source noteuspto-grants-2014_11