反応式
[CH3:1][C:2]1[N:7]=[C:6](/[CH:8]=[N:9]/O)[CH:5]=[CH:4][CH:3]=1.C(O)(=O)C>[Zn].C(O)C>[CH3:1][C:2]1[N:7]=[C:6]([CH2:8][NH2:9])[CH:5]=[CH:4][CH:3]=1参加物
実験手順
To (E)-6-methylpicolinaldehyde oxime (0.635 g, 4.66 mmol)/acetic acid (267 μL, 4.66 mmol)/ethanol (10 mL) solution was added portionwise zinc dust (5.19 g, 79 mmol) over 30 min. The resulting mixture was stirred for additional 30 min. LCMS of reaction aliquot indicated reaction was completed. The zinc precipitates in reaction mixture was removed by filtration, and the filtrate was concentrated. The residue was basified to pH>12 with excess sat. KOH (˜7 mL), and stirred with Et2O (30 mL). The Et2O layer was collected, dried over Na2SO4, and concentrated. The residue was redissolved in EtOAc(15 mL), dried over Na2SO4, and concentrated. (6-Methylpyridin-2-yl)methanamine was obtained as a colorless oil (385 mg, 3.15 mmol, 67.6%). LCMS (m/z) 123.2 (MH+) 0.15 min.
後処理
- customLCMS of reaction aliquot indicated reaction
- customThe zinc precipitates in reaction mixture
- customwas removed by filtration
- concentrationthe filtrate was concentrated
- stirringstirred with Et2O (30 mL)
- customThe Et2O layer was collected
- dry with materialdried over Na2SO4
- concentrationconcentrated
- dissolutionThe residue was redissolved in EtOAc(15 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-ff5918e3df0d434fb1571b7256986869
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242996B2
関連ノート
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