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HRID 481729作成日:2026年10月26日

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

https://huagongshe.com/reaction/481729

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US05789394
出典データセットuspto-grants-1998_08
ORD IDord-e14575929f004883b53f134331baef30
出典メモuspto-grants-1998_08