Hydrochloric Acid → 2-Amino-6-methyl-4-oxo-4H-pyran-3-carbonitrile
反応式
[C:1](#[N:5])[CH2:2][C:3]#[N:4].[H-].[Na+].[CH2:8]=[C:9]1[O:13][C:11](=[O:12])[CH2:10]1.Cl>O1CCCC1>[NH2:4][C:3]1[O:13][C:9]([CH3:8])=[CH:10][C:11](=[O:12])[C:2]=1[C:1]#[N:5]参加物
6
実験手順
To a solution of malononitrile (3.3 g, 50 mmol) in 100 ml of anhydrous tetrahydrofuran was added sodium hydride (60%, 2.2 g, 55 mmol) at −10° C. The resulting reaction mixture was stirred for 2 hours. Then diketene (4.2 g, 50 mmol) was added dropwise to the solution. The reaction mixture was allowed to warm to room temperature and continued to stir for 30 minutes. The mixture was neutralized with hydrochloric acid, and then concentrated to give crude product as red solid, which was used in the next step without further purification.
後処理
- customThe resulting reaction mixture
- stirringto stir for 30 minutes
- concentrationconcentrated
- customto give crude product as red solid, which
- customwas used in the next step without further purification
出典と根拠
- ORDレコード
- ord-abba68ae478945f39d9260bfa1a39571
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09206128B2
反応ノート
読み込み中…