反応式
[ClH:1].[C:2](#[N:7])[CH2:3][CH2:4][CH2:5][CH3:6].[CH2:8]([OH:10])[CH3:9]>>[ClH:1].[CH2:8]([O:10][C:2](=[NH:7])[CH2:3][CH2:4][CH2:5][CH3:6])[CH3:9]参加物
反応条件
- 温度
- 0 °C
実験手順
Hydrogen chloride gas was bubbled into a tared solution of valeronitrile (92.0 g, 1.08 mole) in absolute ethanol (64 ml, 1.08 mole) in a 1-liter round bottom flask cooled to 0° C. The flask was weighed periodically and hydrogen chloride gas bubbling was continued until the weight gain was greater than 39 g (1.08 mole). The mixture was then stoppered and stored at 0° C. for 6 days. Ether (650 mi) was then added (cold) and the mixture was stored at -30° C. for 24 hours. The resulting solid was collected on a buchner funnel, transferred quickly to a large beaker, triturated quickly with cold ether, and collected again on a buchner funnel. The solid was then dried in vacuum to give the title F compound as a free flowing white solid (95 g).
後処理
- customhydrogen chloride gas bubbling
- additionEther (650 mi) was then added (cold)
- waitthe mixture was stored at -30° C. for 24 hours
- customThe resulting solid was collected on a buchner funnel
- customtriturated quickly with cold ether
- customcollected again on a buchner funnel
- customThe solid was then dried in vacuum
- customto give the title F compound as
出典と根拠
- ORDレコード
- ord-f946711c2a274f2e960990d792024a36
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05466704
関連ノート
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