Acetic Anhydride → N-(3-Fluoro-4-trifluoromethyl-phenyl)-acetamide

Temperature

23 °C

To a mixture of 3-fluoro-4-trifluoromethyl-phenylamine (16.9 g, 92.6 mmol), N,N-dimethyl-4-aminopyridine (1.13 g, 9.26 mmol), and toluene (230 mL) was added acetic anhydride (13.1 mL, 0.139 mol). The reaction mixture was heated at reflux for 3 h, and stirred at 23° C. for 16 h. The reaction mixture was concentrated and the crude product was dissolved in EtOAc (100 mL). The organic layer was washed with water (40 mL) and brine (40 mL), dried, filtered, and concentrated under reduced pressure. The crude solid was triturated from DCM/hexanes to yield the titled compound (16.5 g, 81% yield). MS (ESI/CI): mass calcd. for C9H7F4NO, 221.1; m/z found, 222.0 [M+H]+. 1H NMR (400 MHz, CDCl3): 7.68 (d, J=12.5 Hz, 1H), 7.52 (t, J=8.3 Hz, 1H), 7.45 (br s, 1H), 7.19 (d, J=8.5 Hz, 1H), 2.22 (s, 3H).

1. temperatureThe reaction mixture was heated
2. temperatureat reflux for 3 h
3. concentrationThe reaction mixture was concentrated
4. dissolutionthe crude product was dissolved in EtOAc (100 mL)
5. washThe organic layer was washed with water (40 mL) and brine (40 mL)
6. customdried
7. filtrationfiltered
8. concentrationconcentrated under reduced pressure
9. customThe crude solid was triturated from DCM/hexanes

ORD record

ord-e00ed7d965f649dcaef2448b5ebb8977

Source dataset

uspto-grants-2014_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08865713B2