Reaktionsgleichung
[NH2:1][CH2:2][CH:3]([OH:5])[CH3:4].[CH3:6][N:7]1[CH2:12][CH2:11][C:10](=O)[CH2:9][CH2:8]1>>[CH3:4][CH:3]1[CH2:2][NH:1][C:10]2([CH2:11][CH2:12][N:7]([CH3:6])[CH2:8][CH2:9]2)[O:5]1Komponenten
3
Versuchsvorschrift
A mixture of 1-amino-2-propanol (9.2 ml, 1.2 mmol) and 1-methyl-4-piperidone (11.5 ml, 1.0 mmol) was heated under reflux for 2 h and left overnight at room temperature. The reaction mixture was distilled under reduced pressure (˜15 mm Hg). The title compound was collected at 82-95° C. 1H NMR (CDCl3, 300 MHz) δ 4.02 (m, 1H, OCH), 3.25 (dd, J=11.9, 6.3 Hz, 1H, CHH), 2.68 (dd, J=11.9, 6.6 Hz, 1H, CHH), 2.4-2.6 (m, 4H-piperidine), 2.1 (s, 3H, NCH3), 1.65-1.81 (m, 4H-piperidine), 1.21 (d, J=6.1 Hz, 3H, CH3CH) ppm.
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 2 h
- distillationThe reaction mixture was distilled under reduced pressure (˜15 mm Hg)
- customThe title compound was collected at 82-95° C
Quellen und Nachweise
- ORD-Eintrag
- ord-911accd4f1464a1281423855fd3d36ce
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09034891B2
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