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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1585649Erstellt: 27. Oktober 2026

1,1-Ethanediol → 2-(3-Chloropropyl)-2-phenyl-1,3-dioxolane

https://huagongshe.com/reaction/1585649

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-EthanediolHCID 151211—
Edukt4-ChlorobutyrophenoneHCID 253533—
Katalysatorp-Toluenesulfonic acidHCID 6101—
LösungsmittelTolueneHCID 1140—
Produkt2-(3-Chloropropyl)-2-phenyl-1,3-dioxolaneHCID 12866338111,6%

Reaktionsschritte

4-Chlorobutyrophenone (15.18 g, 0.083 moles), ethanediol (6.80 g, 0.110 moles) and p-toluene sulphonic acid (0.20 g) were heated in toluene at reflux and water was removed from the reaction using a Dean and Stark apparatus. After 17 hours the solvent was removed by distillation in vacuo to leave crude 2-phenyl-2-(3-chloropropyl)-1,3-dioxolane (21 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05939447
Quelldatensatzuspto-grants-1999_08
ORD IDord-3d2fcc7e27644a48bc71b43e6a7389cd
Quellennotizuspto-grants-1999_08