Reaktionsgleichung
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][CH:8]=[C:9]2[NH:12][C:13](=[O:15])[CH3:14])=[CH:4][CH:3]=1.[H-].[Na+].Cl[CH2:19][CH:20]1[CH2:22][CH2:21]1.O>CS(C)=O>[CH:20]1([CH2:19][O:1][C:2]2[CH:11]=[C:10]3[C:5]([CH:6]=[CH:7][CH:8]=[C:9]3[NH:12][C:13](=[O:15])[CH3:14])=[CH:4][CH:3]=2)[CH2:22][CH2:21]1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
17.1 g (0.085 mol) of N-(7-hydroxynaphth-1-yl)acetamide in solution in 50 ml of dimethyl sulphoxide are added under a nitrogen atmosphere to a suspension of 3.4 g (0.085 mol) of sodium hydride in oil, washed beforehand with dry pentane), in 100 ml of dimethyl sulphoxide, while the mixture is cooled with an ice-water bath. Stirring is continued at room temperature for 2 h. 9.05 g (0.1 mol) of (chloromethyl)cyclopropane are added, and the mixture is stirred at room temperature for 4 h and left to stand overnight. The mixture is poured into 1 l of water, stirred for 1 h and left to stand overnight under cold conditions. The solid is separated by filtration, washed with water and dried. 13 g of a product melting point: 154°-155° C., are obtained which is used as it is in the following step.
Aufarbeitung
- washwashed
- temperaturewhile the mixture is cooled with an ice-water bath
- stirringthe mixture is stirred at room temperature for 4 h
- waitleft
- waitto stand overnight
- stirringstirred for 1 h
- waitleft
- waitto stand overnight under cold conditions
- customThe solid is separated by filtration
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-f7008c6b03ac4d55ada0fd490ad51b40
- Quelldatensatz
- uspto-grants-1996_06
- Patentnummer
- US05530002
Verknüpfte Notizen
Wird geladen…