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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167241생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1167241

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물4-Nitro-m-xyleneHCID 6991—
반응물Chlorosulfonic acidHCID 24638—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물2,4-dimethyl-5-nitro (N,N-dimethyl)benzenesulfonamideHCID 983493537%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06617357B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-cfcef51d76e14bb9b49ffe780ca6a967
출처 메모uspto-grants-2003_09