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HRID 728426作成日:2026年10月27日

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

https://huagongshe.com/reaction/728426

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TetrahydrofuranHCID 8028—
反応物Diphenyl diselenideHCID 15460—
反応物Sodium borohydrideHCID 4311764—
反応物3-(3-Iodopropylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropaneHCID 14835021—
溶媒EthanolHCID 702—
生成物2-Methoxy-1-octadecylcarbamoyloxy-3-(3-phenylselenylpropylsulfonylamino)propaneHCID 13171700098%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05047540
出典データセットuspto-grants-1991_09
ORD IDord-678f8b3ef726451ebd6be9ac672c9a3f
出典メモuspto-grants-1991_09