Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Di-tert-butylchlorophosphine | HCID 139566 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 14906272 | HCID 14906272 | — |
Reaction Steps
A 30 mL of reactor equipped with magnetic stir bar was charged with 50 mg (0.093 mmol) of (t-Bu)2PCl)2PdCl2, 0.50 g (4.4 mmol) of 3-bromopyridine, 0.50 g (3.16 mmol) of Ph2NH and 0.25 g (4.46 mmol) of KOH in 2 mL of 1,4-dioxane. The reaction mixture was refluxed for 5 hours. The reaction mixture was cooled to room temperature, transferred to a separatory funnel, and diluted with 100 mL of diethyl ether and 20 mL of H2O. The layers were separated, and organic layer was washed with H2O (2×50 mL), brine (30 mL), and dried over MgSO4, filtered, and solvents removed from the filtrate by rotary evaporation. The resulting residue was chromatographed on silicon gel. The eluate was concentrated by rotary evaporation followed by high vacuum to give 3-pyridyldiphenylamine. LC-MS Found: 247.3 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06878850B2 |
|---|
| Source dataset | uspto-grants-2005_04 |
|---|
| ORD ID | ord-3d8904ebd9784e21b39b1f82aa075366 |
|---|
| Source note | uspto-grants-2005_04 |
|---|