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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365789생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/365789

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Diethyl (2,2-diethoxyethyl)phosphonateHCID 82071—
반응물Sodium BicarbonateHCID 516892—
반응물1-t-BUTYLDIPHENYLSILYLOXY-3-MERCAPTO-2-PROPANOLHCID 21255877—
용매TolueneHCID 1140—
생성물Trans 5-(t-Butyldiphenylsilyloxymethyl)-2-(Diethyloxyphosphinoylmethyl)-1,3-OxathiolaneHCID 13172078887%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127540
출처 데이터셋uspto-grants-2000_10
ORD IDord-52c5ecdd0fce4c7985b893dbbecb5f66
출처 메모uspto-grants-2000_10