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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359356Erstellt: 25. Oktober 2026

3,4,5-Trimethoxybenzaldehyde → 2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/359356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4,5-TrimethoxybenzaldehydeHCID 6858—
EduktSodium HydroxideHCID 14798—
Edukt3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
LösungsmittelEthanolHCID 702—
Produkt2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanoneHCID 5371610683%

Reaktionsschritte

To a mixture of 2,2,5-trimethyl-3(2H)-furanone (2.5 g, 19.8 mM) and 3,4,5-trimethoxybenzaldehyde (4.7 g, 23.8 mM) in ethanol was added 1N aqueous sodium hydroxide (4 mL, 4mM). After the reaction mixture was stirred for 48 hours at room temperature, the solution was concentrated to 50 mL and diluted with water (300 mL). The aqueous layer was extracted with diethyl ether (4×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a dark yellow crystalline solid. The crude product was purified by chromatography (silica gel, petroleum ether-ethyl acetate) to give light yellow crystals (5.0 g, 83% yield), m.p. 149°-150° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05001126
Quelldatensatzuspto-grants-1991_03
ORD IDord-35d8c43986d044b590463d0e55aa15d7
Quellennotizuspto-grants-1991_03