HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924551Generated: November 2, 2026
Benzene, 1,3-diiodo- → HCID 118112463, compound
https://huagongshe.com/reaction/924551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene, 1,3-diiodo- | HCID 12270 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 118112470 | HCID 118112470 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 118112463 | HCID 118112463 | 63% |
Reaction Steps
6-(10-phenylanthracen-9-yl)-9H-pyrido[2,3-b]indole (1.76 g, 4.19 mmol), 1,3-diiodobenzene (2.76 g, 8.37 mmol), CuI (319 mg, 1.67 mmol), K3PO4 (1.78 g, 8.37 mmol), trans-1,2-dicyclohexanediamine (0.2 mL, 1.67 mmol) were put in a 250 mL two-neck flask and dissolved in 1,4-dioxane. The solution was refluxed and stirred at 120° C. for 12 hours. After completion of the reaction, the solution was extracted with methylenechloride and H2O and was distilled under reduced pressure to remove the solvent. The resultant was columned with a solution of hexane and methylenechloride (1:5). The solution was re-crystallized in a solution of methylene chloride and petroleum ether such that the white solid compound was obtained, (1.66 g, yield: 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09281482B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-8e91105b5a164a4892d7b1566ebfe449 |
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| Source note | uspto-grants-2016_03 |
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