HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924550Generated: October 31, 2026
p-Diiodobenzene → HCID 118112467, compound
https://huagongshe.com/reaction/924550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Diiodobenzene | HCID 12208 | — |
| 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 118112467 | HCID 118112467 | 64% |
Reaction Steps
6-(10-phenylanthracen-9-yl)-9H-pyrido[2,3-b]indole (1.76 g, 4.19 mmol), 1,4-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/H2O and distilled under reduced pressure to remove the solvent. The resultant was columned with a solution of n-hexane and methylenechloride (1:5) and was re-crystallized in a solution of methylene chloride and petroleum ether such that the solid compound was obtained, (1.67 g, yield: 64%).
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-d713d9f32d3548b1ba71cc73b963731f |
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| Source note | uspto-grants-2016_03 |
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