Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanesulfonyl chloride → N-(4-bromo-2-ethylphenyl)methanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 4-Bromo-2-ethylaniline | HCID 2801283 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(4-bromo-2-ethylphenyl)methanesulfonamide | HCID 6469152 | 81% |
반응 단계
4-Bromo-2-ethyl-aniline (2 mL, 14 mmol) dissolved in anhydrous pyridine (35 mL) at toom temperature was treated with methylsulfonyl chloride (1.3 mL, 16.8 mmol). The reaction was stirred at that temperature for 15 hours before it was diluted with EtOAc. The mixture was washed with H2O, brine and dried over MgSO4. The solvent was removed in vacuo and the residue was purified with flash chromatography (SiO2, 5–30% EtOAc in hexanes) to afford the desired product (3.1 g, 81% yield). 1H NMR (300 MHz, CDCl3): δ 1.25 (t, J=7.5 Hz, 3 H), 2.61–2.68 (m, 2 H), 3.02 (s, 3 H), 6.36 (s, 1 H), 7.36–7.39 (m, 3 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07151105B2 |
| 출처 데이터셋 | uspto-grants-2006_12 |
| ORD ID | ord-389a00c858154614be5cd1adf398aead |
| 출처 메모 | uspto-grants-2006_12 |