Reaktionsgleichung
[F:1][C:2]([F:11])([F:10])[CH2:3][CH2:4][CH:5]([C:8]#[N:9])[C:6]#[N:7].[H-].[Na+].[C:14]([C:17]1[CH:24]=[CH:23][C:20]([CH2:21]Br)=[CH:19][CH:18]=1)(=[O:16])[CH3:15]>CN(C)C=O>[C:14]([C:17]1[CH:24]=[CH:23][C:20]([CH2:21][C:5]([CH2:4][CH2:3][C:2]([F:10])([F:11])[F:1])([C:8]#[N:9])[C:6]#[N:7])=[CH:19][CH:18]=1)(=[O:16])[CH3:15]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Using 0.3 g of (3,3,3-trifluoropropyl)malononitrile, 3 ml of N,N-dimethylformamide, 0.08 g of sodium hydride (60% in oil), and 0.4 g of 4-acetylbenzyl bromide, and according to the process described in the Production Example 1, there was obtained 0.43 g of 2-(4-acetylbenzyl)-2-(3,3,3-trifluoropropyl)malononitrile (the present compound (6)).
Quellen und Nachweise
- ORD-Eintrag
- ord-b959e0b912e0481d9446d9479abfd2e8
- Quelldatensatz
- uspto-grants-2008_07
- Patentnummer
- US07402691B2
Verknüpfte Notizen
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