HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521541Generated: October 30, 2026
Water → 4,4'-(3,3'-bipyridine-6,6'-diyl)bis(N,N-diphenylaniline)
https://huagongshe.com/reaction/521541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(5-bromopyridin-2-yl)-N,N-diphenylaniline | HCID 66799571 | — |
| Reactant | N,N-diphenyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)aniline | HCID 66801665 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4'-(3,3'-bipyridine-6,6'-diyl)bis(N,N-diphenylaniline) | HCID 56943729 | 82% |
Reaction Steps
A mixture of 1 (3.05 g, 7.59 mmol), 2 (3.40 g, 7.59 mmol), tetrakis(triphenylphosphine)palladium(0) (0.438 g, 0.379 mmol), Na2CO3 (7.42 g, 70.0 mmol), H2O (70 mL) and THF (115 mL) was degassed with argon for about 1.25 h while stirring. The stirring reaction mixture was then maintained under argon at 80° C. for about 65 h. Upon confirming consumption of the starting materials by TLC (SiO2, CH2Cl2), the reaction was cooled to room temperature (RT) and poured over CH2Cl2 (400 mL). The organics were then washed with sat. NaHCO3, H2O and brine, dried over MgSO4, filter and concentrated in vacuo. Purification of the crude product via flash chromatography (SiO2, 100% CH2Cl2 to 49:1 CH2Cl2-acetone) provided 3 (3.98 g, 82% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328086B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-96680b552ae745bdbabc0883f47086a8 |
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| Source note | uspto-grants-2016_05 |
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