反応式
O=[C:2]([CH2:8][C:9](=[O:11])[CH3:10])[C:3]([O:5][CH2:6][CH3:7])=[O:4].Cl.[CH3:13][O:14][NH2:15]>C(O)C.ClCCl>[CH3:13][O:14][N:15]=[C:2]([CH2:8][C:9](=[O:11])[CH3:10])[C:3]([O:5][CH2:6][CH3:7])=[O:4]参加物
5
実験手順
A mixture of ethyl 2,4-dioxopentanoate (10.9 g, 68.7 mmol) and N-methoxyamine hydrochloride (4.01 g, 48.1 mmol) in ethanol (40 ml) was left to stand over molecular sieves 3A (25 g) for 18 h and diluted with dichloromethane (25 ml) The sieves was removed by filtration and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography eluting with 5% ethyl acetate/n-hexane to give the title compound (12.9 g, 34%).
後処理
- waitwas left
- customwas removed by filtration
- concentrationthe filtrate was concentrated under vacuum
- customThe residue was purified by silica gel chromatography
- washeluting with 5% ethyl acetate/n-hexane
出典と根拠
- ORDレコード
- ord-b4b1ee3a41174507ba3942db2b2a29f1
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07897607B2
関連ノート
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