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HRID 1013092Erstellt: 25. Oktober 2026

Dimethyl Sulfate → 5-Methoxy-1,4-dihydronaphthalene

https://huagongshe.com/reaction/1013092

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktPotassium CarbonateHCID 11430—
Edukt5,8-Dihydro-1-naphtholHCID 97466—
LösungsmittelEthanolHCID 702—
Produkt5-Methoxy-1,4-dihydronaphthaleneHCID 1513106692,5%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Add powdered potassium carbonate (193.1 g, 1.397 mol) to a solution of commercially available 5,8-dihydronaphthalen-1-ol [68.08 g, 90% potency based on 1H-NMR, 0.4657 mol, from Societa Italiana Medicinala Scandicci, s.r.l., Reggello (Firenze), Italy] in ethanol (700 mL). Cool the solution to 0° C. with ice water and add dimethyl sulfate (88.1 g, 66.1 mL, 0.699 mol) dropwise, maintaining the temperature between 5° C. and 10° C. Heat the reaction mixture to 40° C. until TLC shows the absence of starting material (about 2 hr). Filter off the solids by vacuum filtration and concentrate. Dilute the residual brown oil with diethyl ether (500 mL), wash with 10% aqueous ammonium hydroxide (500 mL), water (500 mL), brine (500 mL), dry (sodium sulfate) and concentrate to give the crude product as a brown oil (73 g). Purify the crude product by short path distillation under vacuum (bp 120-130° C./5 Torr) to give the title compound as a clear oil (69.0 g, 92.5% potency corrected) (contains some 1,2,3,4-tetrahydro-5-methoxynaphthalene as an impurity).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07981882B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-452ab81680f64905869b3220362db98d
Quellennotizuspto-grants-2011_07