Reaktionsgleichung
[F-:1].[Cs+].[F:3][C:4]([C:12]#[N:13])([C:8]([F:11])([F:10])[F:9])[C:5]([F:7])=[O:6].[F:14][C:15]([C:31]([F:34])([F:33])[F:32])([O:19][C:20]([F:30])([F:29])[C:21]([F:28])(C#N)[C:22]([F:25])([F:24])[F:23])[C:16]([F:18])=[O:17].[F:35][C:36]([F:44])([F:43])[C:37]1([F:42])[O:41][C:38]1([F:40])[F:39]>COCCOCCOCCOCCOC>[F:14][C:15]([C:31]([F:34])([F:33])[F:32])([O:19][C:20]([F:29])([F:30])[C:21]([F:28])([C:22]([F:23])([F:25])[F:24])[O:41][C:38]([F:40])([F:39])[C:37]([F:42])([C:36]([F:44])([F:43])[F:35])[O:6][C:5]([F:1])([F:7])[C:4]([F:3])([C:12]#[N:13])[C:8]([F:9])([F:10])[F:11])[C:16]([F:18])=[O:17]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
By essentially the procedure of Examples 1 and 2, 7 g of cesium fluoride, 30 ml of tetraglyme, 11.5 g of perfluoro(α-cyanopropionyl) fluoride, 68.5 g of perfluoro-(5-cyano-2-methyl-3-oxahexanoyl) fluoride, and 256 g of hexafluoropropylene oxide were reacted to give, in addition to the products of Examples 1 and 2, 24.1 g of perfluoro-11-cyano-2,5,8-trimethyl-3,6,9-trioxadodecanoyl fluoride, B.P. 106°C/100 mm. Spectral data:
Quellen und Nachweise
- ORD-Eintrag
- ord-c33c7f0fa2d84ede9fff3696bf5bb242
- Quelldatensatz
- uspto-grants-1976_01
- Patentnummer
- US03933767
Verknüpfte Notizen
Wird geladen…