HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1847102Erstellt: 26. Oktober 2026
Pentafluoroiodobenzene → 2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenyl
https://huagongshe.com/reaction/1847102
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pentafluoroiodobenzene | HCID 70008 | — |
| Edukt | 2-(2-Methoxy-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 79662121 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Potassium Carbonate | HCID 11430 | — |
| Produkt | 2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenyl | HCID 57327803 | 93% |
Reaktionsschritte
Compound 5 (11.3 g, 45.54 mmol, 1 equiv) and iodopentafluorobenzene (10.6 g, 36.2 mmol, 1 equiv) were dissolved in toluene (200 mL) and 1.0M potassium carbonate solution (200 mL). Tetrabutylammonium bromide (1.6 g, 5 mmol, 0.11 equiv) was added and the solution sparged with nitrogen for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (2.63 g, 2.28 mmol, 0.05 equiv) was added and the reaction was refluxed for one day. The reaction was cooled to room temperature, then the layers were separated. The aqueous phase was back extracted with ethyl acetate (2×200 mL). Combined organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified over silica gel (200 g), eluting with heptanes to give 2,3,4,5,6-pentafluoro-2′-methoxy-5′-methyl-1,1′-biphenyl (6) (9.7 g, 74% yield) as a pale-yellow oil. This material contained a small amount of unreacted iodopentafluorobenzene which was identified by 19F NMR. The material was used subsequently.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08952114B2 |
|---|
| Quelldatensatz | uspto-grants-2015_02 |
|---|
| ORD ID | ord-e95ef93340a349c391c502c27ec4471d |
|---|
| Quellennotiz | uspto-grants-2015_02 |
|---|