HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilylacetylene → Tris(4-((trimethylsilyl)ethynyl)phenyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Tris(4-bromophenyl)amine | HCID 258027 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Diisopropylamine | HCID 7912 | — |
| Product | Tris(4-((trimethylsilyl)ethynyl)phenyl)amine | HCID 23443707 | 81% |
Reaction Steps
Thereafter, to 200 ml of diisopropylamine were added 15.54 g (0.032 mol of tri(4-bromophenyl)amine, 1.35 g (1.92 mmol) of bis[triphenylphosphin]palladium dichloride and 9.43 g (0.96 mmol) of copper iodide. After the reaction mixture was stirred for 2 h at room temperature, 9.43 g, (96 mmol) of trimethylsilyl acetylene was slowly added to the reaction mixture. The reaction mixture was refluxed for 8 h and cooled. Solvent was removed under the reduced pressure. The residue was extracted with benzene and the benzene layer was washed with distilled water. The washed benzene layer was concentrated to give 13.84 g (81%) of tri(4-trimethylsilylethynylphenyl)amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06682782B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-c28251a72e284fd682b010ce47b24c90 |
| Source note | uspto-grants-2004_01 |