Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Nitrophenyl methyl sulfide → (Rs)-s-methyl-s-(4-nitrophenyl)-n-tosylsulphimide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Nitrophenyl methyl sulfide | HCID 96109 | — |
| 반응물 | chloramine-T trihydrate | HCID 517414 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (Rs)-s-methyl-s-(4-nitrophenyl)-n-tosylsulphimide | HCID 59683178 | 22% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07943629B2 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-46e8fd89e72b42cfa50550d8d73a9ec4 |
| 출처 메모 | uspto-grants-2011_05 |