化工社化工社 化学情報印刷レポート · 研究参考用
2-Bromoethyl methyl ether → Methyl 2-(2-methoxyethyl)tricyclo[3.3.1.13,7]decane-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromoethyl methyl ether | HCID 80972 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | Methyl tricyclo[3.3.1.13,7]decane-2-carboxylate | HCID 12600018 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 2-(2-methoxyethyl)tricyclo[3.3.1.13,7]decane-2-carboxylate | HCID 89498778 | — |
反応手順
To a solution of EXAMPLE 56A (0.314 g) in tetrahydrofuran (5 mL) was added dropwise lithium diisopropylamide (1.401 mL) at −78° C. The reaction mixture was stirred for 60 minutes and 2-bromoethyl methyl ether (0.562 g) was added. The reaction mixture was slowly warmed up to room temperature, stirred at room temperature overnight, quenched with saturated aqueous NH4Cl solution (2 mL), and extracted with ether. The combined organic layer was dried over Na2SO4, filtered, concentrated and purified by flash chromotography (silica 40 g, 0%-30% ethyl acetate/hexanes).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08889675B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-974c7881d77149fd9fb57a810cf7c4c9 |
| 出典メモ | uspto-grants-2014_11 |