Reaktionsgleichung
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]([CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1)[NH2:6].[C:16](OC(=O)C)(=[O:18])[CH3:17]>>[C:16]([NH:6][C:5]1[CH:4]=[C:3]([C:2]([F:14])([F:15])[F:1])[CH:9]=[C:8]([C:10]([F:11])([F:12])[F:13])[CH:7]=1)(=[O:18])[CH3:17]Komponenten
3
Versuchsvorschrift
A solution of 3,5-bis(trifluoromethyl)aniline (1.28 g, 5 mmol, Aldrich) in acetic anhydride (5 mL) was stirred at room temperature for 12 h, then all of the solvent was removed to give 1.479 g (98%) of 1-acetamido-3,5-bis(trifluoromethyl)benzene as white needles. 1H NMR (CDCl3): δ 2.229 (s, 3H); 7.589 (s, 1H); 8.048 (s, 2H).
Aufarbeitung
- customall of the solvent was removed
Quellen und Nachweise
- ORD-Eintrag
- ord-caf773cb9d654064bdbcdf75a7a27d40
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05620979
Verknüpfte Notizen
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