HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetone → O-Terphenyl
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Neopentyl glycol | HCID 31344 | — |
| Edukt | (4-Propylphenyl)boronic acid | HCID 4100861 | — |
| Edukt | Trimethyl(2,3,2'-trifluoro-4'-iodobiphenyl-4-yl)silane | HCID 11304300 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | O-Terphenyl | HCID 6766 | 89% |
Reaktionsschritte
A solution of (2 mmol) of 8, (2.2 mmol) of 4-propylphenylboronic acid, 250 mg (2.40 mmol) of neopentyl glycol, 1.53 g (4.84 mmol) of Ba(OH)2 8 H2O, 1.35 ml (0.103 mmol, 5 mol %) of a 76 mM acetone solution of Pd(OAc)2 in 20 ml of 95% i—PrOH is stirred at 80° C. for 12 hours. The solvent is subsequently removed under reduced pressure. 5 ml of 2 M HCl are added to the residue, and the mixture is extracted with dichloromethane (3×5 ml). The combined organic phases are dried over MgSO4 and filtered through SiO2. The solvent is removed under reduced pressure, and the residue is converted into 10 (yield: 89%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07842845B2 |
| Quelldatensatz | uspto-grants-2010_11 |
| ORD ID | ord-de98e425693a48bca8f2833cf7957733 |
| Quellennotiz | uspto-grants-2010_11 |