反応式
[C:1]([C:3]1[O:4][CH:5]=[CH:6][CH:7]=1)#[N:2].C[O-].[Na+].[C:11](O)(=[O:13])C>CO>[O:4]1[CH:5]=[CH:6][CH:7]=[C:3]1[C:1](=[NH:2])[O:13][CH3:11]参加物
5
実験手順
2-Cyanofuran (4.50 g, 48.3 mmol) was dissolved in methanol (25 ml), and sodium methoxide (130 mg, 2.4 mmol) was added under ice-cooling. The mixture was stirred while the temperature is slowly raised up to room temperature for 2 hours. After the reaction was completed, acetic acid (0.16 g, 2.6 mmol) was added to neutralize the reaction solution, and the solution was concentrated under reduced pressure. Diethyl ether (100 ml) was added to the concentrated residue, and insolubles were removed by filtration The filtrate was concentrated under reduced pressure to give the crude product of methyl 2-furancarboximidate (6.0 g) as a pale yellow oil.
後処理
- temperaturecooling
- concentrationthe solution was concentrated under reduced pressure
- additionDiethyl ether (100 ml) was added to the concentrated residue, and insolubles
- customwere removed by filtration The filtrate
- concentrationwas concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-9c806235fd5c46b2ac9b7b989cd20b7f
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05272164
関連ノート
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