HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 90387091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | HCID 59866480 | HCID 59866480 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 90387091 | HCID 90387091 | 91.2% |
Reaction Steps
4-(3-bromophenyl)dibenzo[b,d]thiophene (9.00 g, 26.5 mmol), sodium iodide (7.95 g, 53.1 mmol), copper(I) iodide (1.516 g, 7.96 mmol), and dioxane (265 ml) were added into a 500 mL 3-necked flask. N1,N2-dimethylcyclohexane-1,2-diamine (2.092 ml, 13.26 mmol) was added. The mixture was degassed by bubbling nitrogen for 30 minutes and the reaction mixture was heated and refluxed overnight. After completion of the reaction, the heating was stopped and the mixture was filtered through a pad of Celite® and washed several times with DCM. The crude material was purified via column chromatography using hexane/DCM (80/20). The target 4-(3-iodophenyl)dibenzo[b,d]thiophene (9.33 g, 24.16 mmol, 91% yield) was afforded as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927749B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-4f7ba487c26b4031bcc5d72c41a2f2b6 |
| Source note | uspto-grants-2015_01 |