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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4-(5-bromopyridin-2-yl)-N,N-diphenylanilineHCID 66799571—
ReactantN,N-diphenyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)anilineHCID 66801665—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4,4'-(3,3'-bipyridine-6,6'-diyl)bis(N,N-diphenylaniline)HCID 5694372982%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328086B2
Source datasetuspto-grants-2016_05
ORD IDord-96680b552ae745bdbabc0883f47086a8
Source noteuspto-grants-2016_05