HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 7H-Dibenzo(a,g)carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57655345 | HCID 57655345 | — |
| Reactant | 7-acetyl-12-bromo-7H-dibenzo [a,g]carbazole | HCID 71277894 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7H-Dibenzo(a,g)carbazole | HCID 9160 | — |
Reaction Steps
Following the above procedure, Suzuki coupling of 3.8 g of 7-acetyl-12-bromo-7H-dibenzo [a,g]carbazole and 2.7 g of (4-benzo[d]thiazol-2-yl) phenylboronic acid were stirred together in 30 ml of toluene. To this was added 0.02 g of tetrakis(triphenylphosphine)palladium, 2.1 g of potassium carbonate and 10 ml of aqueous ethanol were added and refluxed under nitrogen for 6 h. The reaction was quenched with water and the toluene layer was removed and passed through a celite column. The organic layers were combined and then evaporated in a rotary evaporator under vacuum to yield 4.1 g of 7-acetyl-12-[4-benzo[d]thiazol-2-yl) phenyl]-7H-dibenzo[a,g]carbazole as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353085B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-6cbb5b4bfd664254a9e8b69ce020987c |
| Source note | uspto-grants-2016_05 |