Reaktionsgleichung
C([N:3]([CH2:6][CH3:7])CC)C.[C:8]([O:11][C:12](=O)[CH3:13])(=O)[CH3:9].[CH2:15](Cl)Cl>>[CH3:9][C:8]1[O:11][C:12]([CH2:7][CH2:6][NH2:3])=[CH:13][CH:15]=1Komponenten
4
Versuchsvorschrift
To a solution of the amine C (1 mol) in CH2Cl2 (approx. 10 ml per 1 g of the starting compound) triethylamine (1.1 mol) and acetic anhydride (1.2 mol) were added. The reaction mixture is stirred at room temperature for 1 h and concentrated on rotary evaporator. The residue is triturated with hexane, filtered, washed with hexane to give a crystalline compound in good yields.
Aufarbeitung
- concentrationconcentrated on rotary evaporator
- customThe residue is triturated with hexane
- filtrationfiltered
- washwashed with hexane
- customto give a crystalline compound in good yields
Quellen und Nachweise
- ORD-Eintrag
- ord-fecd54f676ab45f1abfe9f1bb1307074
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07947689B2
Verknüpfte Notizen
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