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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470909Generated: October 27, 2026

Potassium Phosphate, Tribasic → 1-Phenyl-2-(5-benzo[c]phenanthren-4-ylphenyl)benzimidazole

https://huagongshe.com/reaction/1470909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-(4-Bromophenyl)-1-phenyl-1H-benzo(d)imidazoleHCID 23094070—
ReactantBenzo[c]phenanthren-5-ylboronic acidHCID 59622711—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product1-Phenyl-2-(5-benzo[c]phenanthren-4-ylphenyl)benzimidazoleHCID 86659546—

Reaction Steps

913 mg (3 mmol) of tri-o-tolylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a vigorously stirred suspension of 17.5 g (50 mmol) of 1-phenyl-2-(4-bromophenyl)benzimidazole, 14.9 g (55 mmol) of benzo[c]phenanthrene-5-boronic acid and 25.5 g (120 mmol) of tripotassium phosphate in a mixture of 300 ml of toluene, 100 ml of dioxane and 400 ml of water, and the mixture is subsequently heated under reflux for 16 h. After the mixture has been cooled, the precipitated solid is filtered off with suction, washed three times with 50 ml of toluene, three times with 50 ml of ethanol:water (1:1, v:v) and three times with 100 ml of ethanol and recrystallised three times from DMF (about 7 ml/g). Yield: 16.8 g (34 mmol), 67.8%, purity 99.9% (HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006503B2
Source datasetuspto-grants-2015_04
ORD IDord-781e17af8f2c4c1aa92614ee463179d8
Source noteuspto-grants-2015_04