Reaktionsgleichung
[C:1]1([NH2:11])[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>CCO>[C:1]1([NH:11][C:12](=[O:14])[CH3:13])[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of commercially available 5,6,7,8-tetrahydro-naphthylamine (2 g, 14 mmol) in EtOH (5 mL) at rt was slowly added acetic anhydride (1.28 mL, 13.6 mmol). After addition, the reaction mixture was stirred at rt for 5 min. The resulting suspension was filtered, the collected solid washed with hexane (5×) and dried under vacuum to furnish the title compound (2.5 g) as an off-white solid.
Aufarbeitung
- customat rt
- additionAfter addition
- filtrationThe resulting suspension was filtered
- washthe collected solid washed with hexane (5×)
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-ae08502f027e4a19971bc0af285062d9
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07772267B2
Verknüpfte Notizen
Wird geladen…