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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548957생성일: 2026년 10월 25일

4-Nitrophenyl methyl sulfide → (Rs)-s-methyl-s-(4-nitrophenyl)-n-tosylsulphimide

https://huagongshe.com/reaction/548957

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitrophenyl methyl sulfideHCID 96109—
반응물chloramine-T trihydrateHCID 517414—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물(Rs)-s-methyl-s-(4-nitrophenyl)-n-tosylsulphimideHCID 5968317822%

반응 단계

10.0 g (35.3 mmol) of chloramine-T trihydrate (Aldrich) are added to 5.0 g (29.6 mmol) of 1-methylsulphanyl-4-nitrobenzene in 120 ml of acetonitrile at room temperature. The mixture is stirred at room temperature for 4 hours and then diluted with ethyl acetate. The mixture is filtered with suction and the filter cake is washed with ethyl acetate. The combined organic phases are dried (Na2SO4), filtered and concentrated. The resulting residue is recrystallized from methanol. 2.2 g (6.5 mmol; yield: 22%) of the product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943629B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-46e8fd89e72b42cfa50550d8d73a9ec4
출처 메모uspto-grants-2011_05