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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 481729Erstellt: 25. Oktober 2026

p-Toluenesulfonic acid → Trans 5-(t-Butyldiphenylsilyloxymethyl)-2-(Diethyloxyphosphinoylmethyl)-1,3-Oxathiolane

https://huagongshe.com/reaction/481729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktDiethyl (2,2-diethoxyethyl)phosphonateHCID 82071—
EduktSodium BicarbonateHCID 516892—
Edukt1-t-BUTYLDIPHENYLSILYLOXY-3-MERCAPTO-2-PROPANOLHCID 21255877—
LösungsmittelTolueneHCID 1140—
ProduktTrans 5-(t-Butyldiphenylsilyloxymethyl)-2-(Diethyloxyphosphinoylmethyl)-1,3-OxathiolaneHCID 13172078887%

Reaktionsschritte

To a solution of diethylphosphonoacetaldehyde diethylacetal (12.23 g, 48.1 mmol, 1.2 eq.) and t-butyldiphenylsilyloxy-3-mercapto-2-propanol (13.63 g, 38.1 mmol, 1.2 eq.) in toluene (500 mL) was added PTSA (0.73 g, 3.8 mmol, 0.1 eq.). The mixture was stirred at reflux for 72 hr and was cooled to room temperature. A saturated solution of sodium bicarbonate was added and the aqueous phase was extracted with dichloromethane. The organic phase was dried with anhydrous magnesium sulphate and evaporated under reduced pressure. The crude material was purified by flash chromatography with ethyl acetate:hexane (2:1), and gave 16.31 g of the compound in a 87% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05789394
Quelldatensatzuspto-grants-1998_08
ORD IDord-e14575929f004883b53f134331baef30
Quellennotizuspto-grants-1998_08