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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728426생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/728426

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물TetrahydrofuranHCID 8028—
반응물Diphenyl diselenideHCID 15460—
반응물Sodium borohydrideHCID 4311764—
반응물3-(3-Iodopropylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropaneHCID 14835021—
용매EthanolHCID 702—
생성물2-Methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propaneHCID 13171700098%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05047540
출처 데이터셋uspto-grants-1991_09
ORD IDord-678f8b3ef726451ebd6be9ac672c9a3f
출처 메모uspto-grants-1991_09