Acetaldehyde, 2,2-dimethoxy- → (R)-N-(2,2-dimethoxyethyl)-3-methylbutan-2-amine
反応式
[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH:4]=O.[CH3:8][CH:9]([CH3:13])[C@H:10]([NH2:12])[CH3:11]>CO.[Pd].O>[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH2:4][NH:12][C@@H:10]([CH:9]([CH3:13])[CH3:8])[CH3:11]参加物
6
実験手順
2,2-Dimethoxyacetaldehyde (60% in water, 8.7 mL) was added to (R)-3-methylbutan-2-amine (5.0 g) in methanol (25 mL) and the mixture stirred at ambient temperature overnight. A slurry of palladium on carbon (5%, 1.2 g) in water (10 mL) was added and the mixture was hydrogenated at 5 bar pressure with stirring for 3 hours. The mixture was filtered through Celite and the filter pad washed with methanol (3×100 mL). The combined filtrate and washings were concentrated to a volume of ˜10 mL and then toluene (200 mL) was added. The mixture was concentrated, more toluene (200 mL) was added and the mixture was concentrated once more to give the titled compound as a yellow oil. Yield 8.0 g.
後処理
- stirringwith stirring for 3 hours
- filtrationThe mixture was filtered through Celite
- washthe filter pad washed with methanol (3×100 mL)
- concentrationThe combined filtrate and washings were concentrated to a volume of ˜10 mL
- additiontoluene (200 mL) was added
- concentrationThe mixture was concentrated
- additionmore toluene (200 mL) was added
- concentrationthe mixture was concentrated once more
出典と根拠
- ORDレコード
- ord-974ee83c24e440bb929fea77392c0a3b
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08455483B2
反応ノート
読み込み中…