Methylamine → Methyl(4-(3-pyridyloxy)butyl)amine
反応式
Cl[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1.[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1参加物
反応条件
- 温度
- 100 °C
実験手順
The 4-chloro-1-(3-pyridyloxy)butane (2.00 g, 10.8 mmol) was dissolved in methanol (25 mL) and added to a 40 wt % aqueous solution of methylamine (50 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 4 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (10 mL) was added to the residue, and the solution (pH 6) was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was basified to pH 10 with 10% NaOH solution, and the mixture was extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 1.47 g (75.5%) of an oil.
後処理
- customThe tube was sealed
- temperatureAfter cooling
- concentrationthe mixture was concentrated by rotary evaporation
- additionSaturated NaCl solution (10 mL) was added to the residue
- extractionthe solution (pH 6) was extracted with ether (3×25 mL)
- customto remove impurities
- extractionthe mixture was extracted with chloroform (4×25 mL)
- dry with materialThe combined chloroform extracts were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporation to a residue that
- customwas dried briefly under high vacuum
出典と根拠
- ORDレコード
- ord-6af7c7e26e0c4710abf1a85608fb1dc9
- 出典データセット
- uspto-grants-2003_09
- 特許番号
- US06627648B1
反応ノート
読み込み中…