Reaktionsgleichung
[C:1]([C:4]1[O:5][CH:6]=[CH:7][CH:8]=1)(=[O:3])[CH3:2].[F:9][C:10]([F:23])([F:22])[C:11]([F:21])([F:20])[C:12]([F:19])([F:18])[C:13](OCC)=[O:14]>>[F:18][C:12]([F:19])([C:11]([F:20])([F:21])[C:10]([F:9])([F:22])[F:23])[C:13](=[O:14])[CH2:2][C:1]([C:4]1[O:5][CH:6]=[CH:7][CH:8]=1)=[O:3]Komponenten
3
Versuchsvorschrift
The compound was synthesized according to example 1 using 2-acetylfuran and ethyl heptafluorobutyrate as starting materials. 1H NMR (CDCl3): 6.54 (s, 1 H); 6.65 (dd, 1H, J=1.6 & 3.6 Hz); 7.37 (dd, 1H, J=0.6 & 3.6 Hz); 7.70 (dd, 1H, J=0.6 & 1.6 Hz). IR (film): 1616 (C═O); 1231 (C—F).
Aufarbeitung
- customThe compound was synthesized
Quellen und Nachweise
- ORD-Eintrag
- ord-f3fccfb5c8a044b0aa0d637faa113401
- Quelldatensatz
- uspto-grants-2008_06
- Patentnummer
- US07381567B2
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