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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375535Generated: October 29, 2026

Triethylamine → 4-[4-(4-Phenylpiperazin-1-yl)but-1-ynyl]benzaldehyde

https://huagongshe.com/reaction/375535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant1-(But-3-yn-1-yl)-4-phenylpiperazineHCID 18993038—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-[4-(4-Phenylpiperazin-1-yl)but-1-ynyl]benzaldehydeHCID 1899304660.3%

Reaction Steps

A mixture of 4-bromobenzaldehyde (4.05 g), 1-but-3-ynyl-4-phenylpiperazine (Step A) (4.69 g), triethylamine (9.2 mL), bis (triphenylphosphine)palladium dichloride (0.31 g) and copper (I) iodide (0.08 g) in acetonitrile (100 mL) is degassed with nitrogen and stirred at room temperature for 16 hours. The solvent is evaporated and the residue is dissolved in dichloromethane (200 mL), washed with 2N sodium carbonate (150 mL), dried over MgSO4, filtered and evaporated to leave a brown oil. This oil is purified by MPLC on silica gel eluting with 15% then 30% ethyl acetate (EtOAc)/hexanes to give 4.2 g of the title compound as a yellow waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486517
Source datasetuspto-grants-1996_01
ORD IDord-0a202009b66243b29e703b8e6f171c06
Source noteuspto-grants-1996_01