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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233418Erstellt: 25. Oktober 2026

4-Hydroxybenzaldehyde → 4-(4-[6-Acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehyde

https://huagongshe.com/reaction/233418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HydroxybenzaldehydeHCID 126—
EduktWaterHCID 962—
Edukt4-((6-(Acryloyloxy)hexyl)oxy)benzoic acidHCID 3713565—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4-[6-Acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehydeHCID 2335580092,4%

Reaktionsschritte

0.6 g of N,N'-dicyclodicyclohexylcarbodiimide is added at room temperature while stirring to a solution of 1.0 g of 4-[6-acryloyloxyhexyloxy]benzoic acid, 0.3 g of 4-hydroxybenzaldehyde and 0.04 g of 4-dimethylaminopyridine in 20 ml of dichloromethane. The reaction mixture is stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of dichloromethane each time. The combined organic phases are washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and the filtrate is subsequently concentrated. Chromatographic purification of the residue on silica gel with hexane/ethyl acetate (vol. 1:1) and two-fold recrystallization from ethanol of the fractions which are pure according to thin-layer chromatography gives 0.9 g of 4-(4-[6-acryloyloxyhexyloxy]phenylcarbonyloxy)benzaldehyde.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05593617
Quelldatensatzuspto-grants-1997_01
ORD IDord-953181295d8246269c1c0e0eba1ecf74
Quellennotizuspto-grants-1997_01