Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Allyl Alcohol → N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Allyl Alcohol | HCID 7858 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-(3-iodophenyl)methanesulfonamide | HCID 21830928 | — |
| 촉매 | Palladium Chloride | HCID 24290 | — |
| 촉매 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamide | HCID 57444373 | 60.5% |
반응 단계
A mixture of N-(3-iodo-phenyl)-methanesulfonamide (2.4 g, 8 mmol), tetra-n-butyl-ammonium chloride (2.22 g, 8 mmol), allyl alcohol (0.7 g, 12 mmol), sodium hydrogencarbonate (1.6 g, 19 mmol) and palladium(II) chloride (0.36 g, 1.8 mmol) in anhydrous dimethylformamide (30 mL) was stirred at room temperature for 48 h under argon. The mixture was then diluted with 5% aqueous hydrochloric acid (100 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layers were dried (sodium sulfate) and evaporated in vacuo. The crude product was purified by silica gel chromatography (ethyl acetate in hexane, 30% to 50%) to give the title compound as an amber oil (1.1 g, 60%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07732600B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-c3abfdc781784af8ae3f38b4d5d92de5 |
| 출처 메모 | uspto-grants-2010_06 |