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HRID 365789作成日:2026年10月27日

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

https://huagongshe.com/reaction/365789

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Diethyl (2,2-diethoxyethyl)phosphonateHCID 82071—
反応物Sodium BicarbonateHCID 516892—
反応物1-t-BUTYLDIPHENYLSILYLOXY-3-MERCAPTO-2-PROPANOLHCID 21255877—
溶媒TolueneHCID 1140—
生成物Trans 5-(t-Butyldiphenylsilyloxymethyl)-2-(Diethyloxyphosphinoylmethyl)-1,3-OxathiolaneHCID 13172078887%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06127540
出典データセットuspto-grants-2000_10
ORD IDord-52c5ecdd0fce4c7985b893dbbecb5f66
出典メモuspto-grants-2000_10