Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 6-Bromo-2-nitropyridin-3-ol | HCID 21873808 | — |
| 촉매 | Ethyl bromoacetate | HCID 7748 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate | HCID 59560649 | 89% |
반응 단계
2-Bromo-5-hydroxy-6-nitropyridine (30 g, 0.14 mole) was suspended in acetone (200 ml), and potassium carbonate (39 g, 0.28 mole) was added, followed by ethyl bromoacetate (15.7 ml, 0.14 mmole). The reaction was heated at reflux for 10 hr, then was cooled to room temperature and diluted with Et2O. The precipitate was removed by suction filtration, and the filtrate was concentrated in vacuo to afford material (38 g, 89%), which was used without further purification; MS (ES) m/z 305.0 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07592334B2 |
| 출처 데이터셋 | uspto-grants-2009_09 |
| ORD ID | ord-8f12ba2a98ac4a69b32475207f3a49ea |
| 출처 메모 | uspto-grants-2009_09 |