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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231275Generated: October 25, 2026

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

https://huagongshe.com/reaction/231275

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Sulfanylbutan-1-olHCID 548261—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Methoxy-3-octadecyloxypropyl methanesulfonateHCID 14501037—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-3-octadecyloxypropyl 4-hydroxybutyl sulfideHCID 53941631—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845219
Source datasetuspto-grants-1989_07
ORD IDord-bacae9d55f0144cdbdc047a7c7c98359
Source noteuspto-grants-1989_07