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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9255Erstellt: 24. Oktober 2026

Acetone → 2,6-Diallyl4-benzyloxyphenol

https://huagongshe.com/de/reaction/9255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktMonobenzoneHCID 7638—
EduktAllyl bromideHCID 7841—
EduktPotassium CarbonateHCID 11430—
Produkt2,6-Diallyl4-benzyloxyphenolHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091230B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1782f4c6e18d44388356e24fbc39135b
Quellennotizuspto-grants-2006_08