Reaktionsgleichung
[CH:1]([C:3]1[C:4](=[O:10])[NH:5][C:6](=[O:9])[NH:7][CH:8]=1)=[CH2:2].[Br-:11]>CN(C)C=O>[Br:11]/[CH:2]=[CH:1]/[C:3]1[C:4](=[O:10])[NH:5][C:6](=[O:9])[NH:7][CH:8]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5-vinyluracil (2.75 g, 20 mmoles) was dissolved in dry dimethylformamide (250 ml). To this solution was added a solution of bromide (3.2 g, 20 mmoles) in dry dimethylformamide (30 ml). The reaction mixture was shaken until colourless and then heated at 100° for 1 hour. The solution was then evaporated under reduced pressure to a brown oil to which was added water (30 ml). The resulting pink suspension was filtered and the pale pink solid recrystallised from methanol to give E-5-(2-bromovinyl)uracil (3.62 g, 84% yield).
Aufarbeitung
- temperaturethen heated at 100° for 1 hour
- customThe solution was then evaporated under reduced pressure to a brown oil to which
- additionwas added water (30 ml)
- filtrationThe resulting pink suspension was filtered
- customthe pale pink solid recrystallised from methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-c1f745ea3eba4373895683c13b299593
- Quelldatensatz
- uspto-grants-1984_01
- Patentnummer
- US04424211
Verknüpfte Notizen
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