Methyl iodide → Ethyl 5-chloro-1-methyl-1H-indole-2-carboxylate
反応式
[H-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:7]2.[CH3:18]I>CN(C)P(=O)(N(C)C)N(C)C>[Cl:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH3:18])[C:8]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:7]2参加物
実験手順
8.7 gm (0.2 mol) of a 55% dispersion of sodium hydride in oil were added over a period of 15 minutes at a temperature of 0° C. and in a nitrogen atmosphere to a solution of 40.0 gm (0.18 mol) of ethyl 5-chloro-indole-2-carboxylate in 150 ml of hexamethyl-phosphoric acid triamide. After stirring the resulting mixture for 2.5 hours at room temperature, 35.5 gm (0.25mol) of methyl iodide were added dropwise, while cooling. After stirring overnight, 1200 ml of ice water were added to the mixture, while externally cooling on an ice bath. The aqueous mixture was then extracted 5 times with 150 ml of ether each. The combined ether extracts were washed with water 5 times, dried over magnesium sulfate, and evaporated in vacuo. The raw product was then recrystallized from petroleum ether, yielding 35.8 gm (85% of theory) of ethyl 5-chloro-1-methyl-indole-2-carboxylate. M.p.: 81.5°-82° C.
後処理
- temperaturewhile cooling
- stirringAfter stirring overnight
- temperaturewhile externally cooling on an ice bath
- extractionThe aqueous mixture was then extracted 5 times with 150 ml of ether each
- washThe combined ether extracts were washed with water 5 times
- dry with materialdried over magnesium sulfate
- customevaporated in vacuo
- customThe raw product was then recrystallized from petroleum ether
出典と根拠
- ORDレコード
- ord-aeb2a42f51004d7a96f1f4bb6c00d7b0
- 出典データセット
- uspto-grants-1979_01
- 特許番号
- US04137313
反応ノート
読み込み中…