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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805966Generated: November 1, 2026

Potassium Carbonate → 2-[4-(2,8-diphenyldibenzothiophen-4-yl)phenyl]-1-phenyl-1H-benzimidazole

https://huagongshe.com/reaction/1805966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-(4-Bromophenyl)-1-phenyl-1H-benzo(d)imidazoleHCID 23094070—
Reactant2,8-Diphenyldibenzothiophen-4-boronic acidHCID 58309671—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product2-[4-(2,8-diphenyldibenzothiophen-4-yl)phenyl]-1-phenyl-1H-benzimidazoleHCID 58309550—

Reaction Steps

In a 50-mL three-neck flask were put 1.8 g (5.0 mmol) of 2-(4-bromophenyl)-1-phenyl-1H-benzimidazole, 2.2 g (5.8 mmol) of 2,8-diphenyldibenzothiophen-4-boronic acid, and 76 mg (0.2 mmol) of tri(ortho-tolyl)phosphine. The air in the flask was replaced with nitrogen. To this mixture were added 5.8 mL of a 2.0 mmol/L aqueous solution of potassium carbonate, 19 mL of toluene, and 6 mL of ethanol. Under reduced pressure, this mixture was stirred to be degassed. Then, 11 mg (50 μmol) of palladium(II) acetate was added to this mixture, and the mixture was stirred at 80° C. for 4 hours under a nitrogen stream.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354542B2
Source datasetuspto-grants-2013_01
ORD IDord-3cb554bd555047f69196a35e2e61fae0
Source noteuspto-grants-2013_01