HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tris(4-bromophenyl)amine → 4-(Thiophen-2-yl)-N,N-bis(4-(thiophen-2-yl)phenyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tris(4-bromophenyl)amine | HCID 258027 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Thiophen-2-yl)-N,N-bis(4-(thiophen-2-yl)phenyl)aniline | HCID 15315428 | 85% |
Reaction Steps
First, 1 g (2 mmol) of tris(4-bromophenyl)amine (Aldrich) was dissolved in 100 ml of toluene, and then 2.9 ml (4.5 eq.) of 2-tributylstannylthiophene and 27 mg (1.1%) of Pd(PPh3)4 were added thereto. The mixture was refluxed under a nitrogen atmosphere for 12 hours. The reaction mixture was allowed to cool to room temperature, washed with brine twice, and dried over MgSO4. After the solvent was evaporated, the obtained residue was washed with petroleum ether (PE), and dried, affording 0.87 g (yield: 85%) of tris[4-(2-thienyl)phenyl]amine as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07731796B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-7c16fafe58124208947e5b9c94c8c2d7 |
| Source note | uspto-grants-2010_06 |