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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 634876Erstellt: 23. Oktober 2026

Hydroquinone → 4-(Dec-9-enyloxy)phenol

https://huagongshe.com/de/reaction/634876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
EduktPotassium HydroxideHCID 14797—
Edukt10-Bromo-1-deceneHCID 543384—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4-(Dec-9-enyloxy)phenolHCID 1586077736,4%

Reaktionsschritte

Hydroquinone (37.65 g, 342 mmol) and dec-9-enyl bromide (25 g, 114 mmol) were dissolved in ethanol (150 ml) with warming under a nitrogen atmosphere. The solution was heated under reflux and a solution of potassium hydroxide (6.83 g, 121 mmol) in water (20 ml) was added dropwise over 1 h. The resulting suspension was heated under reflux (3 H) then poured on to water (500 ml) and extracted with ether (3×100 ml). The combined extracts were dried (MgSO4), evaporated in vacuo and the residue extracted with heptane (300 ml). On cooling, it afforded a first crop of the phenol (10.31 g). The remaining material was chromatographed (flash grade silica gel, petroleum ether 40-60° C./diethyl ether 3/2). 2 was isolated as white plates (Rf=0.57). Combined yield=15.61 g (55%). Mp=54° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06184322B2
Quelldatensatzuspto-grants-2001_02
ORD IDord-fb73047467264b8d946e2a5e2cc96875
Quellennotizuspto-grants-2001_02