反応式
[C-:1]1([CH:6]=O)[CH:5]=[CH:4][CH:3]=[CH:2]1.[CH-:8]1[CH:12]=[CH:11][CH:10]=[CH:9]1.[Fe+2:13].[CH3:14][NH2:15].[BH4-].[Na+]>C1COCC1.CO>[CH3:14][NH:15][CH2:6][C-:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[CH-:8]1[CH:12]=[CH:11][CH:10]=[CH:9]1.[Fe+2:13]参加物
6
実験手順
A solution of ferrocenecarboxaldehyde (700 mg, 3.27 mmol) and methylamine (2.0M in THF) (5.0 ml, 10.0 mmol) in THF (25 ml) and methanol (30 ml) was stirred at room temperature for 15 h under a nitrogen atmosphere. Sodium borohydride (371 mg, 9.81 mmol) was added to the solution and it was stirred at room temperature for 1 h. The solvent was removed out under reduced pressure and the residue dissolved in chloroform. The chloroform was washed with water, dried over magnesium sulphate. The solvent was removed under reduced pressure to yield a brown oil (647 mg, 86%).
後処理
- customThe solvent was removed out under reduced pressure
- dissolutionthe residue dissolved in chloroform
- washThe chloroform was washed with water
- dry with materialdried over magnesium sulphate
- customThe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-b94a4a2f3e4448a68a13a414c8786a03
- 出典データセット
- uspto-grants-2003_12
- 特許番号
- US06664407B2
関連ノート
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