Morpholine → 4-{4-[2-Chloroethoxy]benzoyl}morpholine
Reaktionsgleichung
[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=[O:10])=[CH:7][CH:6]=1.[NH:14]1[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1>C(Cl)Cl>[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([N:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)=[O:10])=[CH:7][CH:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-(2-Chloroethoxy)benzoyl chloride (5.0 g) was dissolved in dry methylene chloride and stirred while cooling to 0°. Morpholine (4.0 g) was added dropwise and the mixture was stirred at room temperature for 2 days. The resultant colourless solid was filtered off and the liquors allowed to stand from which the title compound crystallised (5.5 g), m.p. 102°-104°.
Aufarbeitung
- temperaturewhile cooling to 0°
- stirringthe mixture was stirred at room temperature for 2 days
- filtrationwas filtered off
- customcrystallised (5.5 g), m.p. 102°-104°
Quellen und Nachweise
- ORD-Eintrag
- ord-8e850304df9d4f539f10dfc4c73051f1
- Quelldatensatz
- uspto-grants-1992_01
- Patentnummer
- US05079248
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