Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 4-Allyloxy-3-nitrocinnamic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Malonic Acid | HCID 867 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 4-Allyloxy-3-nitrobenzaldehyde | HCID 22401152 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 4-Allyloxy-3-nitrocinnamic acid | HCID 54381117 | 70.3% |
반응 단계
4-Allyloxy-3-nitrobenzaldehyde (5 g, 24.1 mM) was dissolved in pyridine (100 ml) and malonic acid (5.02 g, 48.3 mM) and piperidine (0.48 ml, 4.8 mM) added. The mixture was heated to reflux with stirring for 2 hours, cooled, and poured onto a mixture of concentrated hydrochloric acid and ice. Organics were extracted into ethyl acetate, the organic layer washed with 2M hydrochloric acid, and product back-extracted into aqueous NaHCO3. The aqueous solution was then re-acidified (concentrated hydrochloric acid), and organics extracted into ethyl acetate, washed with brine, and dried (MgSO4), to give title compound (4.23 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05527791 |
| 출처 데이터셋 | uspto-grants-1996_06 |
| ORD ID | ord-2d00ecb238134095b6b0426401ec41a6 |
| 출처 메모 | uspto-grants-1996_06 |