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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 322606Erstellt: 27. Oktober 2026

Acetone → 3,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcohol

https://huagongshe.com/reaction/322606

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktPotassium CarbonateHCID 11430—
Edukt3,5-Dihydroxybenzyl alcoholHCID 34661—
Edukt3,5-Bis(4-vinylbenzyloxy)benzyl bromideHCID 18433945—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
Produkt3,5-Di(3,5-di(4-vinylbenzyloxy)benzyloxy)benzylalcoholHCID 1843394481,9%

Reaktionsschritte

A 250 ml flask is charged with 15 g (34.5 mmol, 2.2 eq) of bromide (2) and acetone (100 ml) under an argon atmosphere. To this solution is added 3,5-dihydroxybenzyl alcohol (2.2 g, 15.7 mmol), 0.82 g (31. mmol, 0.2 eq) 18-C-6 and 4.77 g (34-5 mmol, 2.2 eq) of K2CO3 and the mixture is stirred for 48 hours whereupon a yellow suspension is formed. To the mixture is added methylene chloride (200 ml) and water (200 ml). The organic phase is separated, dried over MgSO4 and evaporated to dryness. A dark brown oil is obtained which is dissolved in toluene (40 ml) and hexane (20 ml). Upon cooling, a white powder forms which is collected by filtration to give 10.92 g (81.9% of (3A).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211316B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-7c38a8d86c804a088e9b4407bbaf07ed
Quellennotizuspto-grants-2001_04