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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1955438Erstellt: 26. Oktober 2026

2-(3-Chloropropyl)-2-methyl-1,3-dioxolane → 1,3-Dioxolane, 2-(3-methoxypropyl)-2-methyl-

https://huagongshe.com/reaction/1955438

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(3-Chloropropyl)-2-methyl-1,3-dioxolaneHCID 80079—
EduktSodiumHCID 5360545—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
Produkt1,3-Dioxolane, 2-(3-methoxypropyl)-2-methyl-HCID 560002—

Reaktionsschritte

To a solution of sodium methoxide prepared by the addition of 0.8 g of sodium to 35 mL of methanol was added 5-chloro-2-pentanone ethylene ketal (3 g, 180 mmol). The mixture was heated in a steel bomb at 100° C. for 18 hours. The methanol was removed by evaporation under reduced pressure and the residue was extracted into 20 mL of ether. The ether extract was washed with water, saturated saline solution and dried over magnesium sulfate. Evaporation of the ether yielded 1.6 grams of 5-methoxy-2-pentanone ethylene ketal. This was stirred in 10 mL of 75% formic acid for 24 h at room temperature. The mixture was neutralized with sodium bicarbonate and extracted with 50 mL of ether. The ether extract was washed with water, saturated saline solution and dried over magnesium sulfate. Evaporation yielded 1.2 g of the desired ketone as an oil. Step B: Preparation of 1-(R)-(3,4-dihydroxyphenyl)-2-(1-methyl-4-methoxybutylamino)ethanol oxalate salt

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05775329
Quelldatensatzuspto-grants-1998_07
ORD IDord-9d35a6cce01e443d8b276bda37d566ef
Quellennotizuspto-grants-1998_07