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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 1-Butyl-4-ethynylbenzene | HCID 2775132 | — |
| Reactant | 1-Bromo-4-(4-n-propylphenylethynyl)naphthalene | HCID 67117851 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(4-n-Butylphenylethynyl)-4-(4-n-propylphenylethynyl)naphthalene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08747695B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-c8d6a1e4633540f19073da98de7a307e |
|---|
| Source note | uspto-grants-2014_06 |
|---|