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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521555Generated: October 30, 2026

Water → HCID 56943928, compound

https://huagongshe.com/reaction/521555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant6,6'-Dibromo-3,3'-bipyridineHCID 6426300—
Reactant9-Phenyl-9H-carbazole-3-boronic acidHCID 51358450—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56943928HCID 5694392864.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of (9-phenyl-9H-carbazol-3-yl)boronic acid (1.41 g, 4.92 mmol), 6,6′-dibromo-3,3′-bipyridine (0.750 g, 2.39 mmol), tetrakis(triphenylphosphine)palladium(0) (0.166 g, 0.143 mmol), Na2CO3 (1.59 g, 15.0 mmol), H2O (15 mL) and THF (25 mL) was degassed with argon for about 25 min while stirring. The reaction mixture was then maintained at about 85° C. under argon. Upon confirming consumption of the starting material by thin layer chromatography (TLC) (SiO2, dichloromethane), the reaction was cooled to RT and poured over CH2Cl2 (ca. 350 mL). The organics were then washed with saturated NaHCO3, H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude via flash chromatography (SiO2, 100% CH2Cl2 to 29:1 CH2Cl2-acetone) afforded Compound 22 (0.98 g, 64%) as an off-white solid. MS (ES+) m/z: 639 (C46H30N4 requires 639).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328086B2
Source datasetuspto-grants-2016_05
ORD IDord-31654eb5c7a4484880602cbfbbe8df0e
Source noteuspto-grants-2016_05