Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | HCID 67498142 | HCID 67498142 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67497910 | HCID 67497910 | — |
Reaction Steps
After charging 4.6 parts of 1-phenyl-3,5-di(4-bromophenyl)pyrazoline synthesized by a known method, 2.4 parts of trimethylsilylacetylene, 0.46 parts of tetrakis(triphenylphosphine)palladium(0), 0.038 parts of copper iodide and 20 ml of triethylamine in 40 ml of THF, the mixture was stirred at 66° C. for 8 hours and then the reaction mixture was filtered and washed with THF. The obtained filtrate was concentrated, and the precipitate was filtered, washed, recrystallized from methanol and dried at 60° C. to obtain 4.4 parts of 1-phenyl-3,5-di(4-trimethylsilylethynylphenyl)pyrazoline having a melting point of 108-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08168796B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-3e28aefd8ca748a89f7195588923ef62 |
|---|
| Source note | uspto-grants-2012_05 |
|---|