HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Chlorotoluene → 4-Methylbiphenyl
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Chlorotoluene | HCID 7810 | — |
| Edukt | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Edukt | HCID 178419127 | HCID 178419127 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Produkt | 4-Methylbiphenyl | HCID 12566 | — |
Reaktionsschritte
An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (4.5 mg, 0.015 mmol, 1.5 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), additive (3.0 mmol), and 4-chlorotoluene (0.12 mL, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (2 mL) was added through a rubber septum. The reaction mixture was stirred at room temperature for 20 hours. The reaction mixture was then diluted with ethyl acetate (30 mL) and poured into a separatory funnel. The mixture was washed with 2.0M NaOH (20 mL), followed by brine (20 mL). The organic layer was submitted for GC analysis giving the results tabulated below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07560582B2 |
| Quelldatensatz | uspto-grants-2009_07 |
| ORD ID | ord-f6158e24870b494ca233a54b9fc4989e |
| Quellennotiz | uspto-grants-2009_07 |