Reaktionsgleichung
[OH-].[Na+].[CH2:3]([CH:5]([CH2:8][CH3:9])[CH:6]=[O:7])[CH3:4].[Cl:10][C:11]1[CH:18]=[CH:17][C:14]([CH2:15]Cl)=[CH:13][CH:12]=1>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[Cl:10][C:11]1[CH:18]=[CH:17][C:14]([CH2:15][C:5]([CH2:8][CH3:9])([CH2:3][CH3:4])[CH:6]=[O:7])=[CH:13][CH:12]=1Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
300 ml of toluene, 400 ml of 30 percent (by weight) sodium hydroxide solution and 5.0 g of tetra-n-butyl-ammonium iodide are heated at 80° C. while stirring. To this is slowly added dropwise a mixture of 110 g (1.10 mol) of 2-ethylbutanal and 161 g (1.00 mol) of 4-chlorobenzyl chloride. The mixture is then stirred at 80° C. for 4 h and at room temperature for 14 h, 1,000 ml of toluene are added, and the phases are separated. The organic phase is washed with water, dried over Na2SO4 and concentrated. Fractional distillation results in 123 g (54% of theory) of 2-(4-chlorobenzyl) -2-ethylbutanal as a colorless liquid of boiling point 146°-148° C. at 1 mbar.
Aufarbeitung
- additionTo this is slowly added dropwise
- stirringThe mixture is then stirred at 80° C. for 4 h and at room temperature for 14 h
- customthe phases are separated
- washThe organic phase is washed with water
- dry with materialdried over Na2SO4
- concentrationconcentrated
- distillationFractional distillation
- customresults in 123 g (54% of theory) of 2-(4-chlorobenzyl) -2-ethylbutanal as a colorless liquid of boiling point 146°-148° C. at 1 mbar
Quellen und Nachweise
- ORD-Eintrag
- ord-b9ac554c1e4446a69a6e51b89084bc63
- Quelldatensatz
- uspto-grants-1993_11
- Patentnummer
- US05266579
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