Reaktionsgleichung
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6]/[N:7]=[C:8](/[CH3:14])\[CH:9](OC)OC)=[CH:4][CH:3]=1.[OH-].[Na+]>>[Cl:1][C:2]1[CH:16]=[C:15]2[C:5](=[CH:4][CH:3]=1)[CH:6]=[N:7][C:8]([CH3:14])=[CH:9]2Komponenten
Reaktionsbedingungen
- Temperatur
- 140 °C
Versuchsvorschrift
During 10 min. (4-chloro-benzyl)-[2,2-dimethoxy-1-methyl-eth-(Z)-ylidene]-amine (120 g, 0.496 mol) was added dropwise to polyphosphoric acid (1000 g) at 130° C. The resulting reaction mixture was heated for 3 h at 140° C. After cooling below 100° C. the reaction mixture was poured onto ice (1 kg) and neutralized (pH=7) with a 33% aqueous NaOH solution. Care was taken that the temperature did not rise above 35° C. by adding additional ice. The reaction mixture was extracted with dichloromethane (3×1 L) and the combined organic layers were dried over Na2SO4, filtered and concentrated at reduced pressure to afford a black oil. The crude product was purified bulb-to-bulb distillation (105-110° C., 2 mbar) to afford the title compound as colorless oil which crystallized upon standing (66.7 g, 0.375 mol, 76%). MS (ES+): 178 (M(C10H835ClN)+H)+.
Aufarbeitung
- customThe resulting reaction mixture
- temperatureAfter cooling below 100° C. the reaction mixture
- customdid not rise above 35° C.
- additionby adding additional ice
- extractionThe reaction mixture was extracted with dichloromethane (3×1 L)
- dry with materialthe combined organic layers were dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated at reduced pressure
- customto afford a black oil
- customThe crude product was purified
- distillationbulb-to-bulb distillation (105-110° C., 2 mbar)
Quellen und Nachweise
- ORD-Eintrag
- ord-efc49bb6fa794b66bd7d5bf0fbdbd089
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07781438B2
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