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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117821Generated: October 30, 2026

Ethylenediaminetetraacetic Acid → Carbonylbis[3-(2-pyridyl)benzene]

https://huagongshe.com/reaction/2117821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediaminetetraacetic AcidHCID 6049—
Reactant2-BromopyridineHCID 7973—
ReactantBis(3-bromophenyl)methanoneHCID 12731928—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductCarbonylbis[3-(2-pyridyl)benzene]HCID 2313581275.8%

Reaction Conditions

Temperature-70 °C

Reaction Steps

In a nitrogen atmosphere, a n-pentane solution of t-butyllithium (17.8 ml, 1.60M, 28.5 mmol) was dropwise added to tetrahydrofuran cooled to −70° C., then a tetrahydrofuran (5 ml) solution of 2-bromopyridine (1.2 ml, 12.9 mmol) was added thereto while 15 minutes, after a dropwise, the mixture was stirred at −70° C. for 30 minutes. Then, a tetrahydrofuran solution of zinc chloride (31.8 ml, 0.50 M, 15.9 mmol) was added to the mixture while 10 minutes. Thereafter, the temperature of the reaction mixture was allowed to warm to room temperature while 1 hour, tetrakis(triphenylphosphine)palladium (203 mg) and 3,3′-dibromobenzophenone (2.0 g, 5.88 mmol) were successively added thereto, the reaction mixture was stirred under reflux for 18 hours. After the reaction mixture was allowed to cool, then the mixture was poured into a mixture of ethylenediaminetetraacetic acid (7.0 g)/an aqueous saturated sodium hydrogen carbonate solution (210 ml), an organic layer was separated, furthermore an aqueous layer was extracted with toluene. The organic layer was combined, and the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization, thereby obtaining 1.5 g of carbonylbis[3-(2-pyridyl)benzene as white powder. Yield: 75.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442797B2
Source datasetuspto-grants-2008_10
ORD IDord-617ddd39ded6445d8b1148585546c17e
Source noteuspto-grants-2008_10