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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1738686Erstellt: 25. Oktober 2026

Ethanol → 3-Ethoxy-7-methoxy-1,2-dihydronaphthalene

https://huagongshe.com/reaction/1738686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-oneHCID 75582—
EduktEthylorthoformateHCID 53630039—
KatalysatorSulfuric AcidHCID 1118—
Produkt3-Ethoxy-7-methoxy-1,2-dihydronaphthaleneHCID 21844235—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

33.5 g of 6-methoxy-2-tetralone was dissolved in 27.6 ml of ethanol, followed by subsequently adding 37.8 ml of ethyl orthoformate and one drop of concentrated sulfuric acid. The mixture thus prepared was stirred at 100° C. for 4 hours. After distilling off the solvent under a reduced pressure, the resulting residue was subjected to silica gel column chromatography using chloroform as an eluant. Fractions of interest were pooled and concentrated to collect precipitated crystals, thereby obtaining 5.82 g of 3,4-dihydro-2-ethoxy-6-methoxynaphthalene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05962695
Quelldatensatzuspto-grants-1999_10
ORD IDord-57d593158a8a49518757bb74bd1ff41a
Quellennotizuspto-grants-1999_10