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HRID 1167241作成日:2026年10月27日

Dimethylamine → 2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamide

https://huagongshe.com/reaction/1167241

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物4-Nitro-m-xyleneHCID 6991—
反応物Chlorosulfonic acidHCID 24638—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamideHCID 983493537%

反応条件

温度130 °C

反応手順

In a dry flask under argon filled with 2,4-dimethyinitrobenzene (1.0 g, 6.61 mmol), chlorosulfonic acid (5 mL) was added dropwise. The resulting solution was stirred at 130° C. for 4 h, and then the mixture was poured slowly onto ice. A light brown precipitate formed and was isolated by filtration. The solid was dissolved in methanol (20 mL), and dimethylamine (3 mL) was added with stirring. After 15 min, the reaction mixture was diluted with methylene chloride and 1 M HCl. The layers were separated, and the organics were dried and concentrated. Purification of the residue by flash chromatography (15% ethyl acetate/hexanes) provided 2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamide (626 mg, 37%) as a white solid. Anal. Calcd for C10H14N2O4S: C, 46.50; H, 5.46; N, 10.85. Found: C, 46.68; H, 5.25; N, 10.71.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06617357B2
出典データセットuspto-grants-2003_09
ORD IDord-cfcef51d76e14bb9b49ffe780ca6a967
出典メモuspto-grants-2003_09