HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromobenzene → 4-(3'-Bromobiphenyl-3-yl)dibenzothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3-(Dibenzo[b,d]thiophen-4-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 59575355 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(3'-Bromobiphenyl-3-yl)dibenzothiophene | HCID 66974462 | 79.3% |
Reaction Steps
2-(3-(dibenzo[b,d]thiophen-4-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8.80 g, 22.78 mmol) and 1,3-dibromobenzene (21.49 g, 91 mmol) were dissolved in toluene (300 mL), and potassium carbonate (9.44 g, 68.3 mmol) in 50 mL of water and the Pd(PPh3)4 catalyst (0.263 g, 0.228 mmol) were then added. The reaction mixture was degassed and refluxed under N2 overnight. The organic layer was then separated, evaporated and subjected to column chromatography on silica gel, eluted with hexane/DCM 9:1 v/v mixture, providing 4-(3′-bromo-[1,1′-biphenyl]-3-yl)dibenzo[b,d]thiophene (7.5 g, 18.06 mmol, 79% yield) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580399B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-9b3d76d80e424dd29b9bb938ddf6ac45 |
| Source note | uspto-grants-2013_11 |