HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → {4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium trifluoromethanesulfinate | HCID 23690734 | — |
| Reactant | 4-Bromomethylperfluorobiphenyl | HCID 86591121 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | {4-(Pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane | HCID 22186455 | 94% |
Reaction Steps
4-bromomethylperfluorobiphenyl (3.68 g, 9 mmol) and sodium trifluoromethane sulfinate (1.69 g, 10.8 mmol) were dissolved in propionitrile (30 mL), and the resultant solution was subjected to heating under reflux for 12 hours. After the reaction, the solution was cooled to room temperature, and water was added for extraction with ethyl acetate. The organic phase was dried with magnesium sulfate, filtrated, and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography (hexane-ethyl acetate=20:1 to 8:1 to 1:1), and the aimed {4-(pentafluorophenyl)-2,3,5,6-tetrafluorophenyl}(triflyl)methane (3.91 g, 8.46 mmol, 94% yield) was isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07193113B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-0e51210971dc458bb57d161ed8d10517 |
| Source note | uspto-grants-2007_03 |