Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403067Generated: October 26, 2026

Water → 1-(4-n-Butylphenylethynyl)-4-(4-n-propylphenylethynyl)naphthalene

https://huagongshe.com/reaction/403067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHeptaneHCID 8900—
Reactant1-Butyl-4-ethynylbenzeneHCID 2775132—
Reactant1-Bromo-4-(4-n-propylphenylethynyl)naphthaleneHCID 67117851—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product1-(4-n-Butylphenylethynyl)-4-(4-n-propylphenylethynyl)naphthaleneHCID 86762471—

Reaction Steps

2.35 g (6.3 mmol) of 1-bromo-4-(4-n-propylphenylethynyl)naphthalene and 1.33 g (8.4 mmol) of 4-n-butylphenylacetylene are initially introduced in 40 ml of NEt3, 60 mg (0.3 mmol) of copper(I) iodide and 200 mg (0.3 mmol) of bis(triphenylphosphine)palladium(II) chloride are added, and the mixture is refluxed for 18 h. The batch is cooled, water and heptane are added, and the phases are separated. The organic phase is washed with saturated ammonium chloride solution and subsequently with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated in a rotary evaporator. The residue of compound (1) is purified by column chromatography (SiO2, heptane), and the further purification is carried out by recrystallisation from isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08747695B2
Source datasetuspto-grants-2014_06
ORD IDord-c8d6a1e4633540f19073da98de7a307e
Source noteuspto-grants-2014_06