Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:9])[CH2:5][CH2:6][CH:7]=[O:8])[CH3:2].[Br:10]Br>C(OCC)C>[CH2:1]([O:3][C:4](=[O:9])[CH2:5][CH:6]([Br:10])[CH:7]=[O:8])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a 0-5° C. mechanically-stirred solution in diethyl ether (100 mL) of succinaldehydic acid ethyl ester (10.0 g, 77 mmol) was added bromine (3.9 g, 151 mmol) over 2.5 hours. The reaction mixture was stirred for an additional 1.25 hours and the ether was distilled at atmospheric pressure. The remaining yellow oil was distilled (6.0-6.5 mm Hg, bp 95-101° C.) to give 3-bromosuccinaldehydic acid ethyl ester (10.7 g, 66%).
Aufarbeitung
- distillationthe ether was distilled at atmospheric pressure
- distillationThe remaining yellow oil was distilled (6.0-6.5 mm Hg, bp 95-101° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-e27d267f52fb48c582371c116a9045d5
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06310095B1
Verknüpfte Notizen
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