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HRID 238929作成日:2026年10月26日

p-Aminoacetophenone → N-(4-acetylphenyl)methanesulfonamide

https://huagongshe.com/reaction/238929

反応式

関与物質

役割名称HCID仕込み量
反応物p-AminoacetophenoneHCID 7468—
反応物Methanesulfonyl chlorideHCID 31297—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物N-(4-acetylphenyl)methanesulfonamideHCID 68408395%

反応手順

A cooled solution of 4′-aminoacetophenon (10 mmol) in pyridine (10 mL) at 0° C. was treated with methanesulfonyl chloride (15 mmol) and stirred at room temperature for 2 h. The reaction mixture was diluted with H2O and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes to afford 4′-(Methylsulfonylamino)acetophenone (13-5, LJO-298).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642657B2
出典データセットuspto-grants-2014_02
ORD IDord-ce529ee51da142f182b51d887ecae8d4
出典メモuspto-grants-2014_02