HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 17839517, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 17839508 | HCID 17839508 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 17839517 | HCID 17839517 | 34.1% |
Reaction Steps
6,11-Dihydro-5,7,8,9,10,12-hexapropyl-2,3-diiodonaphthacene (0.23 8 g, 0.324 mmol), 2,3-dichloro-5,6-dicyanobenzoquinone (0.081 g, 0.35 mmol) and 1,4-dioxane (2 ml) were charged in a reactor. The mixture was refluxed for 3 hours. After cooling, the precipitates were removed by filtration. The solvent in the mixture was removed in vacuum followed by recrystallization from chloroform/methanol. The orange red title compound (0.081 g) was obtained. The isolation yield was 34%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07901594B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-0a2ae88757314acd8f2e467460477222 |
| Source note | uspto-grants-2011_03 |