化工社化工社 化学情報印刷レポート · 研究参考用
Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 反応物 | Cyclohexane | HCID 8078 | — |
| 反応物 | Magnesium Bromide | HCID 82241 | — |
| 反応物 | N-ethyl-1-naphthalenecarboxamide | HCID 4088726 | — |
| 反応物 | t-Butylperoxy benzoate | HCID 21744378 | — |
| 反応物 | CID 53628100 | HCID 178418400 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide | HCID 19602319 | 33% |
反応手順
A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05994270 |
| 出典データセット | uspto-grants-1999_11 |
| ORD ID | ord-9c54fa92272446849c5eb0d3d0b99cd6 |
| 出典メモ | uspto-grants-1999_11 |