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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728428생성일: 2026년 10월 25일

Triethylamine → 3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane

https://huagongshe.com/reaction/728428

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Chlorobutane-1-sulphonyl chlorideHCID 74212—
반응물2-Methoxy-3-octadecylcarbamoyloxypropylamineHCID 14992262—
용매DichloromethaneHCID 6344—
생성물3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropaneHCID 1483503177%

반응 단계

To a solution of 1.2 g (3 mM) of 2-methoxy-3-octadecylcarbamoyloxypropylamine IVa1 in 24 ml of dichloromethane and 0.5 ml (3.6 mM) of triethylamine is added 0.75 g (3.93 mM) of 4-chlorobutanesulfonyl chloride with ice-cooling and the mixture is stirred at room temperature overnight. The product is isolated with dichloromethane extraction and dichloromethane layer is washed with 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 (3:2) mixture as an eluent. The product is recrystallized from dichloromethane-n-hexane to give 1.28 g (2.305 mM) of 3-(4-chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane IIIa5 as colorless crystals in 77% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05047540
출처 데이터셋uspto-grants-1991_09
ORD IDord-3eaddd452a6a4961beaa3b84ccbf49b8
출처 메모uspto-grants-1991_09