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HRID 15899作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl AlcoholHCID 7858—
反応物Sodium BicarbonateHCID 516892—
反応物N-(3-iodophenyl)methanesulfonamideHCID 21830928—
触媒Palladium ChlorideHCID 24290—
触媒Tetrabutylammonium ChlorideHCID 70681—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamideHCID 5744437360.5%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732600B2
出典データセットuspto-grants-2010_06
ORD IDord-c3abfdc781784af8ae3f38b4d5d92de5
出典メモuspto-grants-2010_06