Epichlorohydrin → 1-Chloro-3-morpholin-4-yl-propan-2-ol
反応式
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH2:7]([CH:9]1[O:11][CH2:10]1)[Cl:8]>C(O)C>[Cl:8][CH2:7][CH:9]([OH:11])[CH2:10][N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1参加物
4
反応条件
- 温度
- 70 °C
実験手順
A mixture of morpholine (2.6 mL, 30 mmol) and epichlorohydrin (2.35 ml, 30 mmol) in ethanol (50 mL) was stirred at 70° C. overnight. After removing the solvent, the residue was diluted with methylene chloride (50 mL). The clear solid precipitated was collected by vacuum filtration to give 1-chloro-3-morpholin-4-yl-propan-2-ol (2.0 g, 37%). 1H NMR (DMSO-d6) δ 3.49 (t, J=4.8 Hz, 2H), 3.60 (t, J=4.6 Hz, 2H), 3.75 (m, 4H, 2×CH2), 4.20 (dd, J=5.2, 12 Hz, 2H), 4.54 (m, 2H), 4.62 (m, 1H, CH), 6.64 (d, J=6.4 Hz, 1H, OH). MS (m/z) 180.2 (M+1).
後処理
- customAfter removing the solvent
- additionthe residue was diluted with methylene chloride (50 mL)
- customThe clear solid precipitated
- filtrationwas collected by vacuum filtration
出典と根拠
- ORDレコード
- ord-d1cc85e0de9a4b85affb09f318feb5bc
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07179910B2
反応ノート
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