Tetrahydrofuran → 2-(Bicyclo[2.2.1]hept-7-yl)ethylamine
反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].O1CCCC1.[CH:12]12[CH:18]([CH2:19][C:20]([NH2:22])=O)[CH:15]([CH2:16][CH2:17]1)[CH2:14][CH2:13]2>O>[CH:15]12[CH:18]([CH2:19][CH2:20][NH2:22])[CH:12]([CH2:17][CH2:16]1)[CH2:13][CH2:14]2参加物
5
実験手順
0.0425 Mole of lithium aluminum hydride is dissolved in 100 ml. of anhydrous tetrahydrofuran at 0° C, under nitrogen, and then 0.0425 mole of bicyclo[2.2.1]hept-7-yl acetamide in 100 ml. of anhydrous tetrahydrofuran is added dropwise. The mixture is stirred for about 12 hours at room temperature and then about 10 ml. of water is carefully added to decompose excess lithium aluminum hydride (and complex). The mixture is then filtered and the filtrate then dried with potassium hydroxide pellets; filtered and the filtrate distilled, to remove solvent, affording 2-(bicyclo[2.2.1]hept-7-yl)ethylamine.
後処理
- customat 0° C
- filtrationThe mixture is then filtered
- dry with materialthe filtrate then dried with potassium hydroxide pellets
- filtrationfiltered
- distillationthe filtrate distilled
- customto remove solvent
出典と根拠
- ORDレコード
- ord-b6774ea8d7b94674b29ebc7663e32a37
- 出典データセット
- uspto-grants-1977_12
- 特許番号
- US04064258
反応ノート
読み込み中…