Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclohexylisopropylamine → HCID 54014012, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclohexylisopropylamine | HCID 62386 | — |
| 반응물 | Ethyl trimethylsilylacetate | HCID 77687 | — |
| 반응물 | 11-(3',5'-Bistrifluoromethylbenzyloxy) undeca-4-ene-3-one | HCID 57249347 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | HCID 54014012 | HCID 54014012 | — |
반응 단계
n-Butyl lithium (4.99 mmol) in hexane was added to N-isopropyl cyclohexylamine (0.69 g, 4.88 mmol, Aldrich Chem Co.) in dry tetrahydrofuran (20 ml) at -78° under nitrogen. After 15 mins, ethyl trimethylsilylacetate (0.78 g, 4.88 mmol, Fluka Chem. Co.) was added. After a further 10 mins, 11-(3',5'-bistrifluoromethylbenzyloxy) undeca-4-ene-3-one (1 g, 2.44 mmol) was added and the temperature was allowed to reach room temperature. After conventional work-up and chromatography on silica, ethyl 11-(3',5'-bistrifluoromethylbenzyloxy)-3-ethyl-undeca-2, 4- dienoate was obtained as a mixture of two isomers.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05162367 |
| 출처 데이터셋 | uspto-grants-1992_11 |
| ORD ID | ord-f067143e609144788c135f6d17afa0a3 |
| 출처 메모 | uspto-grants-1992_11 |