化工社化工社 化学情報印刷レポート · 研究参考用
Cyclohexylisopropylamine → HCID 54014012、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cyclohexylisopropylamine | HCID 62386 | — |
| 反応物 | Ethyl trimethylsilylacetate | HCID 77687 | — |
| 反応物 | 11-(3',5'-Bistrifluoromethylbenzyloxy) undeca-4-ene-3-one | HCID 57249347 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | HCID 54014012 | HCID 54014012 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05162367 |
| 出典データセット | uspto-grants-1992_11 |
| ORD ID | ord-f067143e609144788c135f6d17afa0a3 |
| 出典メモ | uspto-grants-1992_11 |