Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1076336Erstellt: 26. Oktober 2026

Epichlorohydrin → 1-(2,3-Epoxypropoxy)-5,8-dihydronaphthalene

https://huagongshe.com/reaction/1076336

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEpichlorohydrinHCID 7835—
EduktSodium HydroxideHCID 14798—
Edukt1,4-DioxaneHCID 31275—
Edukt5,8-Dihydro-1-naphtholHCID 97466—
LösungsmittelWaterHCID 962—
Produkt1-(2,3-Epoxypropoxy)-5,8-dihydronaphthaleneHCID 11052686—

Reaktionsschritte

To a cooled solution of 15 g. (0.1 m.) of 5,8-dihydro-1-naphthol and 13.2 g. (0.14 m.) of epichlorohydrin in 38 ml. of p-dioxane, a cold solution of 4.9 g. of sodium hydroxide in 10 ml. of water is added dropwise. The mixture is refluxed three hours, cooled, and extracted with benzene. The benzene extract is washed with water, dried (MgSO4) and evaporated in vacuo to give 1-(2,3-epoxypropoxy)-5,8-dihydronaphthalene. Distillation of the crude oil at 1.2 mm., b.p. 139°-140°, gives a colorless liquid; λliq.max. film 1250, 910, 840 cm-1 (characteristic epoxy bands), CDCl3 4.13 (-C/H=C/H-), 2.5 - 3.5 (aromatic protons).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03956285
Quelldatensatzuspto-grants-1976_05
ORD IDord-16efeedb38004f988ab3ac6269071188
Quellennotizuspto-grants-1976_05