Reaktionsgleichung
[CH2:1]([N:4]([CH2:18][CH2:19][CH3:20])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8]([C:15](=[O:17])[CH3:16])[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:2][CH3:3].[CH3:21][N:22]([CH:24](N(C)C)N(C)C)[CH3:23]>C1(C)C=CC=CC=1>[CH2:18]([N:4]([CH2:1][CH2:2][CH3:3])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8]([C:15](=[O:17])[CH:16]=[CH:21][N:22]([CH3:24])[CH3:23])[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:19][CH3:20]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 2-(di-n-propylamino)-8-acetyl-1,2,3,4-tetrahydronaphthalene (0.3 g, 1.1 mmol), as prepared in co-pending U.S. application Ser. No. 07/653,583, and tris(dimethylamino)methane (0.32 g, 2.2 mmol) in toluene was heated to reflux for 5 hours and at 60° for 18 hours. An additional aliquot of tris (dimethylamino)methane (0.16 g, 1.1. mmol) was added and the reaction stirred at 60° for an additional 2 hours. The reaction was concentrated to give 2-(di-n-propylamino)-8-[1-oxo-3-(dimethylamino)-prop-2-en-1-yl]-1,2,3,4-tetrahydronaphthalene (0.39 g) as a viscous, orange oil.
Aufarbeitung
- temperatureto reflux for 5 hours and at 60° for 18 hours
- concentrationThe reaction was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-2a4ad5e93190493d9bed5b2fbae26db4
- Quelldatensatz
- uspto-grants-1995_07
- Patentnummer
- US05434174
Verknüpfte Notizen
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