Reaktionsgleichung
[CH2:1]([CH:8]([C:11]#[N:12])[C:9]#[N:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].Br[CH2:16][CH2:17][C:18]([F:22])=[C:19]([F:21])[F:20]>CN(C)C=O>[CH2:1]([C:8]([CH2:16][CH2:17][C:18]([F:22])=[C:19]([F:21])[F:20])([C:9]#[N:10])[C:11]#[N:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Using 0.1 g of benzylmalononitrile, 5 ml of N,N-dimethylformamide, 0.010 g of sodium hydride (60% in oil), and 0.04 g of 4-bromo-1,1,2-trifluoro-1-butene, and according to the process described in the Production Example 1, there was obtained 0.042 g of 2-benzyl-2-(3,4,4-trifluoro-3-butenyl)malononitrile (the present compound (4)).
Quellen und Nachweise
- ORD-Eintrag
- ord-cda3e338e4a246658101ae94a38aba97
- Quelldatensatz
- uspto-grants-2008_07
- Patentnummer
- US07402691B2
Verknüpfte Notizen
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