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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15899생성일: 2026년 10월 23일

Allyl Alcohol → N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamide

https://huagongshe.com/ko/reaction/15899

반응식

참여 물질

역할이름HCID투입량
반응물Allyl AlcoholHCID 7858—
반응물Sodium BicarbonateHCID 516892—
반응물N-(3-iodophenyl)methanesulfonamideHCID 21830928—
촉매Palladium ChlorideHCID 24290—
촉매Tetrabutylammonium ChlorideHCID 70681—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
생성물N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamideHCID 5744437360.5%

반응 단계

A mixture of N-(3-iodo-phenyl)-methanesulfonamide (2.4 g, 8 mmol), tetra-n-butyl-ammonium chloride (2.22 g, 8 mmol), allyl alcohol (0.7 g, 12 mmol), sodium hydrogencarbonate (1.6 g, 19 mmol) and palladium(II) chloride (0.36 g, 1.8 mmol) in anhydrous dimethylformamide (30 mL) was stirred at room temperature for 48 h under argon. The mixture was then diluted with 5% aqueous hydrochloric acid (100 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layers were dried (sodium sulfate) and evaporated in vacuo. The crude product was purified by silica gel chromatography (ethyl acetate in hexane, 30% to 50%) to give the title compound as an amber oil (1.1 g, 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732600B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c3abfdc781784af8ae3f38b4d5d92de5
출처 메모uspto-grants-2010_06