HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[4-(2,8-diphenyldibenzothiophen-4-yl)phenyl]-1-phenyl-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2-(4-Bromophenyl)-1-phenyl-1H-benzo(d)imidazole | HCID 23094070 | — |
| Reactant | 2,8-Diphenyldibenzothiophen-4-boronic acid | HCID 58309671 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[4-(2,8-diphenyldibenzothiophen-4-yl)phenyl]-1-phenyl-1H-benzimidazole | HCID 58309550 | — |
Reaction Steps
In a 50-mL three-neck flask were put 1.8 g (5.0 mmol) of 2-(4-bromophenyl)-1-phenyl-1H-benzimidazole, 2.2 g (5.8 mmol) of 2,8-diphenyldibenzothiophen-4-boronic acid, and 76 mg (0.2 mmol) of tri(ortho-tolyl)phosphine. The air in the flask was replaced with nitrogen. To this mixture were added 5.8 mL of a 2.0 mmol/L aqueous solution of potassium carbonate, 19 mL of toluene, and 6 mL of ethanol. Under reduced pressure, this mixture was stirred to be degassed. Then, 11 mg (50 μmol) of palladium(II) acetate was added to this mixture, and the mixture was stirred at 80° C. for 4 hours under a nitrogen stream.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354542B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-3cb554bd555047f69196a35e2e61fae0 |
| Source note | uspto-grants-2013_01 |