Reaktionsgleichung
[Br:1][CH:2]([CH:5]=[O:6])[CH:3]=[O:4].O.[C:8]1(C)[CH:13]=CC(S(O)(=O)=O)=C[CH:9]=1.CC(O)C>C1CCCCC1>[Br:1][C:2](=[CH:5][O:6][CH:8]([CH3:13])[CH3:9])[CH:3]=[O:4]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 86 °C
Versuchsvorschrift
A mixture of 2-bromomalonaldehyde, para-toluenesulfonic acid monohydrate, 2-propanol and cyclohexane were stirred at 86° C. in flask with a dean-stark trap under azeotropic conditions. Further distillation removed another 40% of the original solvent volume. The mixture was cooled to 0° C., then concentrated in-vacuo, to isolate the title compound (13.2 g). 1H-NMR: 9.16 (s, 1H), 7.65 (s, 1H), 4.51 (m, 1H), 1.47 (d, 6H).
Aufarbeitung
- distillationFurther distillation
- customremoved another 40% of the original solvent volume
- temperatureThe mixture was cooled to 0° C.
- concentrationconcentrated in-vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-e8d5ea4059e54f579482ffe59c821d7e
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07585881B2
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