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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1672411생성일: 2026년 10월 27일

N-acetyl-o-toluidine → 3-Acetamido-4-methylbenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1672411

반응식

참여 물질

역할이름HCID투입량
반응물N-acetyl-o-toluidineHCID 8443—
반응물Chlorosulfonic acidHCID 24638—
반응물2-methoxy-N-phenylacetamideHCID 264222—
용매BenzeneHCID 241—
생성물3-Acetamido-4-methylbenzene-1-sulfonyl chlorideHCID 54594388—

반응 조건

온도10 °C

반응 단계

Chlorosulfonic acid (500 g.) was taken in a three neck round bottom flask equipped with a guard tube and cooled it to 10° C. N-acetyl 2-toluidine (100 g.) was added in small portions maintaining temperature below 10° C. After complete addition of 2-methoxy acetanilide cooling is removed and reaction was brought to 25° C. Reaction mixture was stirred at 25° C. for further 24 hours. After the completion of reaction (TLC), the reaction mixture was poured on ice-water, and the resulting slurry was filtered on buchner funnel. Solid cake on funnel was washed with 500 mL of water and the resulting solid was dried on phosphorus pentoxide in a desiccator to obtain 113.5 grams off white solid. It was found to contain a mixture of two isomers as confirmed from NMR and HPLC; however the desired isomer was obtained by partial crystallization using benzene and used for further experimentation, after the thorough carectorisation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07998981B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-93c966f566a443cc85f54105e5a872b4
출처 메모uspto-grants-2011_08