HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetone → 2,6-Diallyl4-benzyloxyphenol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Monobenzone | HCID 7638 | — |
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Produkt | 2,6-Diallyl4-benzyloxyphenol | HCID 21985951 | — |
Reaktionsschritte
To a solution of starting 4-benzyloxyphenol (20 g) in acetone (800 mL) were added allylbromide (50 mL) and K2CO3 (60 g). The reaction mixture was refluxed overnight. After cooling to the room temperature, the insoluble materials were removed by filtration. The filtrate was concentrated in vac. The residue was partitioned between ethyl ether (500 mL) and 2N aqueous NaOH (200 mL). The organic layer was washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated in vac. to give the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091230B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-1782f4c6e18d44388356e24fbc39135b |
| Quellennotiz | uspto-grants-2006_08 |