Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Iodide → 1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 4'-Hydroxyacetophenone | HCID 7469 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | Ammonia | HCID 222 | — |
| 생성물 | 1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanone | HCID 2200112 | 6.8% |
반응 단계
A mixture of 5.97 g of 4′-hydroxyacetophenone (43.8 mmol), 13.0 g of 1-(3-chloropropyl)-piperidine hydrochloride (65.8 mmol), 12.70 g of potassium carbonate (91.89 mmol), and 3.28 g of sodium iodide (21.9 mmol) in 100 mL dry acetone was stirred at reflux. After 1.5 h, the reaction was cooled to room temperature, filtered and concentrated. Ethyl acetate was added and the white solid that remained was filtered off. The filtrate was concentrated in vacuo and the crude residue was purified via silica gel chromatography using a gradient of ethyl acetate then 400:20:10 ethyl acetate: 7N ammonia in methanol:methanol to yield 583 mg of 1-[4-(3-piperidin-1-ylpropoxy)phenyl]ethanone as an oil. MS m/z 265 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08207168B2 |
| 출처 데이터셋 | uspto-grants-2012_06 |
| ORD ID | ord-b682f420bbec46bfa892f79c2171f154 |
| 출처 메모 | uspto-grants-2012_06 |