Chloromethyl Methyl Ether → HCID 22292751、化合物
反応式
[CH:1]([NH:4][CH:5]([CH3:8])[CH2:6][OH:7])([CH3:3])[CH3:2].[H-].[Na+].[CH3:11][O:12][CH2:13]Cl.C(=O)([O-])O.[Na+]>C1COCC1>[CH:1]([NH:4][CH:5]([CH3:8])[CH2:6][O:7][CH2:11][O:12][CH3:13])([CH3:3])[CH3:2]参加物
実験手順
A THF solution (15 mL) of 2-isopropylamino-1-propanol (1.23 g, 10.5 mmol) was added dropwise to a suspension of sodium hydride (504 mg, 0.29 mmol, 60% oil) in THF (9 mL), and the mixture was stirred at the same temperature for 15 minutes. Next, chloromethyl methyl ether (1.20 mL, 15.8 mmol) was added thereto, and the mixture stirred at room temperature for 45 minutes. An aqueous saturated sodium hydrogencarbonate solution was added to the reaction mixture, and then the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and isopropyl-(2-methoxymethoxy-1-methylethyl)amine (0.91 g; yield 54%) was thus obtained. 1H-NMR (CDCl3) δ(ppm): 1.05 (d, J=6.1 Hz, 3H), 1.06 (d, J=5.3 Hz, 3H), 1.08 (d, J=5.3 Hz, 3H), 2.94 (m, 2H), 3.36 (s, 3H), 3.38 (m, 1H), 3.47 (m, 1H), 4.63 (s, 2H).
後処理
- stirringthe mixture stirred at room temperature for 45 minutes
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with a saturated saline solution
- dry with materialdried over anhydrous sodium sulfate
出典と根拠
- ORDレコード
- ord-f2d48c9713404f2a9f141e60b0d0ff8c
- 出典データセット
- uspto-grants-2005_10
- 特許番号
- US06953785B2
反応ノート
読み込み中…