Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
o-Toluenesulfonyl chloride → 1-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | o-Toluenesulfonyl chloride | HCID 8623 | — |
| 반응물 | 3-Acetylindole | HCID 12802 | — |
| 반응물 | Water ethylacetate | HCID 22728543 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone | HCID 357794 | 78% |
반응 단계
Add 1.0 M t-BuOK (3.0 mL, 0.003 mol) to a stirring solution of 3-acetyl indole (0.478 g, 0.0030 mol) in dry DMF (20 mL) under N2 at ambient temperature and stir for 30 min. Add toluenesulfonyl chloride to this solution and stir the resulting mixture overnight. Pour the reaction into EtOAc—H2O, separate the organic layer and extract several times with H2O wash with brine, dry (MgSO4), filter, and evaporate on the rotary evaporator. Chromatograph on the ISCO eluting with a gradient hexane-EtOAc (0-100%) over 30 minutes to give 0.73 g (78%) of the title compound as a solid: 1H (CDCl3). δ 7.8 (d, 1H), 8.2 (s, 1H), 7.9 (d, 1H), 7.7 (d, 2H), 7.4 (m, 2H), 7.3 (d, 2H), 2.6 (s, 3H), 2.4 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07595339B2 |
| 출처 데이터셋 | uspto-grants-2009_09 |
| ORD ID | ord-0dea3151871241489e90aa87c1b82c56 |
| 출처 메모 | uspto-grants-2009_09 |