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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40794생성일: 2026년 10월 25일

Water → N-(4-(methoxymethoxy)butyl)benzenesulfonamide

https://huagongshe.com/reaction/40794

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물TetrahydrofuranHCID 8028—
반응물4-Amino-1-butanolHCID 25868—
반응물Magnesium monoxideHCID 6850729—
생성물N-(4-(methoxymethoxy)butyl)benzenesulfonamideHCID 58218535—

반응 단계

4-Aminobutanol (700 mg) was dissolved in THF (12.5 mL). To the solution, magnesium oxide (1.58 g), water (3.2 mL), and benzenesulfonyl chloride (1.15 mL) were added, and the mixture was stirred at room temperature for 2 hours. The precipitate was removed by filtration, and washed with chloroform (50 mL). Then, the combined filtrate was concentrated under reduced pressure. To the residue, water (20 mL) was added, and the resultant mixture was then extracted with ethyl acetate (20 mL). The organic layer was washed with brine (20 mL), dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (100% ethyl acetate). The obtained colorless oil (1.48 g) was dissolved in dichloromethane (7.5 mL). To the solution, N,N-diisopropylethylamine (3.43 mL) and chloromethyl methyl ether (1.0 mL) were added, and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (50% ethyl acetate/hexane) to obtain the title compound (1.36 g) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530490B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-affdcf1ff0e949dabdf9591d588d7cf2
출처 메모uspto-grants-2013_09