Reaktionsgleichung
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]([CH2:8][C:9]2[CH:10]=[C:11]([OH:15])[CH:12]=[CH:13][CH:14]=2)[CH2:3]1.[H-].[Na+].[O-]S([O-])(=O)=O.[Na+].[Na+].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CN(C=O)C.CCOCC.O>[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][N:4]([CH2:8][C:9]2[CH:10]=[C:11]([CH:12]=[CH:13][CH:14]=2)[O:15][CH2:1][CH2:2][CH2:3][NH2:4])[CH2:3]1Komponenten
8
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
5.13 g (0.025 mol) of 3-[(3-Methylpiperidin-1-yl) methyl]phenol are introduced into a suspension of 1.0 g (0.025 mol) of sodium hydride (60%) in absolute DMF and stirred overnight at room temperature. After the addition of 2.23 g (0.025 mol) of 3-chloropropionic acid nitrile, the reaction mixture is stirred for 7 hours at 60° C. and then poured into ice water and extracted with ether, and the organic phase is washed with 5% NaOH. After dehydration over Na2SO4, the ethereal phase is introduced dropwise into a suspension of 1.14 g (0.03 mol) of LiAlH4 in absolute ether and then hydrolysed with 2.2 ml of H2O. After filtration and removal of solvent by evaporation under vacuum, 2.96 g of a pale yellow oil are left behind.
Aufarbeitung
- stirringthe reaction mixture is stirred for 7 hours at 60° C.
- extractionextracted with ether
- washthe organic phase is washed with 5% NaOH
- filtrationAfter filtration and removal of solvent
- customby evaporation under vacuum, 2.96 g of a pale yellow oil
- waitare left behind
Quellen und Nachweise
- ORD-Eintrag
- ord-055eb18c1384484c97946551c03e5d3e
- Quelldatensatz
- uspto-grants-1988_02
- Patentnummer
- US04727081
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