Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → Ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Decahydroquinoline | HCID 92911 | — |
| 반응물 | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate | HCID 66794569 | 78.9% |
반응 단계
3.38 mL of Et3N and 1.44 mL (11 mmol) of ethyl 3-chloro-3-oxopropionate are added to a solution of 1.5 mL (10 mmol) of decahydroquinoline in 100 mL of AcOEt. The resulting solution is kept under stirring at reflux for 10 h. Then water is added and the organic phase is separated, the aqueous phase is extracted once again with AcOEt. The organic phases are pooled and they are first washed with 5% solution of NaHCO3 and subsequently with brine, they are dried over anhydrous Na2SO4, they are filtered and the solvent is evaporated under reduced pressure. 2.0 g of a yellow oil are obtained. It is identified as intermediate IIIa.1. Method A: tr: 6.76 min; m/z: 268.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08822452B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-e6a5c0325d5a4f4c8690b3127b1584ef |
| 출처 메모 | uspto-grants-2014_09 |