Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Ethoxalyl chloride | HCID 20884 | — |
| 반응물 | 2-[(Cyclopentylcarbonyl)amino]butanoic acid | HCID 21991259 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 3-[(cyclopentylcarbonyl)amino]-2-oxopentanoate | HCID 21991319 | — |
반응 단계
1.6 g (8 mmol) 2-[(cyclopentylcarbonyl)amino]butanoic acid are suspended in 30 ml tetrahydrofurane and heated to reflux together with 1.91 g (24 mmol) pyridine and a bit of N,N-dimethylaminopyridine. While heating at reflux, 2.19 g (16 mmol) ethyl chloro(oxo)acetate are added dropwise. The reaction mixture is heated at reflux until no more evolution of gas can be observed. After cooling down to room temperature, the reaction mixture is added to ice water and the organic phase extracted with ethyl acetate. The dried organic phase is evaporated to dryness in vacuo, dissolved in ethanol and the solution directly used for the next reaction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087605B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-806f557d0a9c4151b5de0201eb12a922 |
| 출처 메모 | uspto-grants-2006_08 |