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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231275Erstellt: 26. Oktober 2026

4-Sulfanylbutan-1-ol → 2-Methoxy-3-octadecyloxypropyl 4-hydroxybutyl sulfide

https://huagongshe.com/reaction/231275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Sulfanylbutan-1-olHCID 548261—
EduktSodium borohydrideHCID 4311764—
EduktSodium MethoxideHCID 10942334—
Edukt2-Methoxy-3-octadecyloxypropyl methanesulfonateHCID 14501037—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methoxy-3-octadecyloxypropyl 4-hydroxybutyl sulfideHCID 53941631—

Reaktionsschritte

To 40 ml of a methanol solution of sodium methoxide (1 M solution) are added 3.1 g of 4-mercaptobutanol and 0.5 g of sodium borohydride, to which is added dropwise a solution of 4.36 g of 2-methoxy-3-octadecyloxypropyl methanesulfonate in 40 ml of tetrahydrofuran at room temperature with stirring. The mixture is stirred at room temperature for 14 hours and then at 40° C. for 1.5 hours. The solvent is distilled off under reduced pressure and the residue is acidified with hydrochloric acid and extracted with hexane. The extract layer is washed with water, dried and concentrated to leave crude 2-methoxy-3-octadecyloxypropyl 4-hydroxybutyl sulfide. This sulfide is dissolved in 75 ml of dichlromethane, to which 7.6 g of m-chloroperbenzoic acid is added little by little at room temperature with stirring. The mixture is then stirred at room temperature for 1 hour and is filtered to remove precipitates. The filtrate is washed with an aqueous sodium sulfite solution, an aqueous sodium bicarbonate solution and water, dried and concentrated to leave a residue which in turn is purified by silica gel column chromatography to obtain 2.5 g of the captioned compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845219
Quelldatensatzuspto-grants-1989_07
ORD IDord-bacae9d55f0144cdbdc047a7c7c98359
Quellennotizuspto-grants-1989_07