Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1,3-diiodo-HCID 12270—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 118112470HCID 118112470—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 118112463HCID 11811246363%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09281482B2
Source datasetuspto-grants-2016_03
ORD IDord-8e91105b5a164a4892d7b1566ebfe449
Source noteuspto-grants-2016_03