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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Diphenyl diselenide | HCID 15460 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 3-(3-Iodopropylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane | HCID 14835021 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-Methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propane | HCID 131717000 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05047540 |
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| 출처 데이터셋 | uspto-grants-1991_09 |
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| ORD ID | ord-678f8b3ef726451ebd6be9ac672c9a3f |
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| 출처 메모 | uspto-grants-1991_09 |
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