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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 728426Erstellt: 25. Oktober 2026

Acetic Acid → 2-Methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propane

https://huagongshe.com/reaction/728426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTetrahydrofuranHCID 8028—
EduktDiphenyl diselenideHCID 15460—
EduktSodium borohydrideHCID 4311764—
Edukt3-(3-Iodopropylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropaneHCID 14835021—
LösungsmittelEthanolHCID 702—
Produkt2-Methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propaneHCID 13171700098%

Reaktionsschritte

To a solution of 1.52 g (4.9 mM) of diphenyl diselenide in 25 ml of dry ethanol is added 370 mg (9.78 mM) of sodium borohydride with ice-cooling and the mixture is stirred for 30 minutes. To the above mixture are added 0.56 ml (9.78 mM) of acetic acid and a solution of 1.03 g (1.63 mM) of 3-(3-iodopropylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane in 10 ml of tetrahydrofuran and the mixture is stirred at room temperature for 1.5 hours. The product is extracted with ethyl acetate, and the organic layer is washed with 1N-hydrochloric acid, saturated aqueous sodium hydrogencarbonate, and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and evaporated. The residue is purified by the column chromatography on silica gel with a n-hexane-ethyl acetate (2:1) eluent to give 1.06 g (1.60 mM) of 2-methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propane IIa1' as a colorless powder in 98% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05047540
Quelldatensatzuspto-grants-1991_09
ORD IDord-678f8b3ef726451ebd6be9ac672c9a3f
Quellennotizuspto-grants-1991_09