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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Bis(3-bromophenyl)methanone | HCID 12731928 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Carbonylbis[3-(2-pyridyl)benzene] | HCID 23135812 | 75.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442797B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-617ddd39ded6445d8b1148585546c17e |
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| Source note | uspto-grants-2008_10 |
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