反応式
[CH3:1][CH2:2][C:3](=O)[CH2:4][CH2:5][CH2:6][CH3:7].Cl.[NH2:10][OH:11]>CO>[CH3:1][CH2:2][C:3](=[N:10][OH:11])[CH2:4][CH2:5][CH2:6][CH3:7]参加物
4
実験手順
A mixture of (R)-1-azabicyclo 2.2.1!heptan-3-one (U.S. Pat. No. 5,306,718) (2.22 g, 20 mmol) and hydroxylamine hydrochloride (1.39 g, 20 mmol) in MeOH (75 mL) is stirred at 25° C. for 18 hours. The solvent is removed under reduced pressure, the residual solid dissolves in saturated Na2CO3, and is extracted with CHCl3. The organic extracts are dried (Na2CO3), and concentrated to give the oxime. The aqueous layer is concentrated, and re-extracted with CHCl3 to yield additional product.
後処理
- additionA mixture of (R)-1-azabicyclo 2.2.1
- customThe solvent is removed under reduced pressure
- dissolutionthe residual solid dissolves in saturated Na2CO3
- extractionis extracted with CHCl3
- dry with materialThe organic extracts are dried (Na2CO3)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-b4f6dc2691024046afdd859e46ea6258
- 出典データセット
- uspto-grants-1996_05
- 特許番号
- US05514812
関連ノート
読み込み中…