Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232415Erstellt: 24. Oktober 2026

Ethylene Glycol → 2-(3-Ethenylphenyl)-1,3-dioxolane

https://huagongshe.com/de/reaction/232415

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktWaterHCID 962—
Edukt3-VinylbenzaldehydeHCID 39390—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelBenzeneHCID 241—
Produkt2-(3-Ethenylphenyl)-1,3-dioxolaneHCID 10241313—

Reaktionsschritte

To a solution of 3-ethenylbenzaldehyde from Step 1 (3.77 g) and ethylene glycol (1.8 mL) in benzene (40 mL ) was added p-toluenesulfonic acid monohydrate (100 mg). The reaction mixture was heated to reflux for 6 hours. The water produced by the reaction was collected in a Dean-Stark trap. The reaction was allowed to cool to room temperature. The reaction was diluted with NH4OAc buffer and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated. Flash chromatography of the residue using 15% diethyl ether in hexane afforded the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04851409
Quelldatensatzuspto-grants-1989_07
ORD IDord-ceae491d9b0947708fde94b767b24416
Quellennotizuspto-grants-1989_07