Acetic Acid → HCID 86650351, Verbindung
Reaktionsgleichung
Br[CH2:2][C:3]([O:11][CH3:12])=[CH:4][C:5](=[O:10])[C:6]([F:9])([F:8])[F:7].[C:13]([O-:16])(=[O:15])[CH3:14].[K+].C(O)(=O)C>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C(#N)C>[C:13]([O:16][CH2:2][C:3]([O:11][CH3:12])=[CH:4][C:5](=[O:10])[C:6]([F:9])([F:8])[F:7])(=[O:15])[CH3:14]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
24.8 g (0.1 mol) of 5-bromo-1,1,1-trifluoro-4-methoxypent-3-en-2-one, 20 g of potassium acetate, 5 g of tetrabutylammonium bromide and 8 g of acetic acid were stirred in 300 ml of acetonitrile at 40° C. for 20 h. The precipitate was filtered off and the solvent was removed completely under reduced pressure.
Aufarbeitung
- filtrationThe precipitate was filtered off
- customthe solvent was removed completely under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-7f330ea03c0e44b48d5c4db88bd3b0d1
- Quelldatensatz
- uspto-grants-2012_08
- Patentnummer
- US08242313B2
Notizen zur Reaktion
Wird geladen…