反応式
[C:1](#[N:5])[CH2:2][C:3]#[N:4].[CH2:6]([O:8][C:9](OCC)(OCC)[CH3:10])[CH3:7].C(OC(=O)C)(=O)C>>[CH2:6]([O:8][C:9](=[C:2]([C:1]#[N:5])[C:3]#[N:4])[CH3:10])[CH3:7]参加物
4
実験手順
Into a 250-mL 3-necked round-bottom flask, was placed malononitrile (20.4 g, 309.09 mmol, 1.00 equiv) at room temperature. To the resulting mixture was then added 1,1,1-triethoxyethane (50 g, 308.64 mmol, 1.00 equiv), in portions at room temperature. To the resulting mixture was then added acetic anhydride (72 g, 705.88 mmol, 2.28 equiv), in portions at room temperature. The resulting solution was heated to reflux for 3 hr. The resulting mixture was concentrated under vacuum, then cooled with a water/ice bath. The solids were collected by filtration to yield 2-(1-ethoxyethylidene)malononitrile as a white solid.
後処理
- customInto a 250-mL 3-necked round-bottom flask, was placed
- customat room temperature
- customat room temperature
- customat room temperature
- temperatureThe resulting solution was heated
- temperatureto reflux for 3 hr
- concentrationThe resulting mixture was concentrated under vacuum
- temperaturecooled with a water/ice bath
- filtrationThe solids were collected by filtration
出典と根拠
- ORDレコード
- ord-5477a329b1b04fd7853d9aa383ddd7bd
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822447B2
関連ノート
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