Réaction #57509
ord-dfe0619ae872459c9e0030ceb8e4fcb6
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1AutreThe layers were separated
- 2Lavagethe organic layer was washed with water (150 mL) and brine (50 mL)
- 3Séchagedried over Mg2SO4
- 4Filtrationfiltrated
- 5Concentrationconcentrated under reduced pressure
Mode opératoire
A mixture of 4-bromo-2-fluoro-benzonitrile (15.0 g, 75.0 mmol), methanol (30.4 mL, 350 mmol) and potassium carbonate (31.1 g, 225 mmol) in DMF (150 mL) was stirred under argon at 55° C. overnight. At this point TLC (100% methylene chloride) revealed no starting material, and the reaction mixture was poured into ether (300 mL) and water (150 mL). The layers were separated, and the organic layer was washed with water (150 mL) and brine (50 mL), dried over Mg2SO4, filtrated, and concentrated under reduced pressure, providing (15.2 g, 95.5%) of 4-bromo-2-methoxy-benzonitrile as a white solid. 1H-NMR (CDCl3) δ 7.41 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 1.6 Hz, 1H), 7.13 (d, J=1.6 Hz, 1H), 3.93 (s, 3H); MS GC-MS (M+=211; RT=6.15 min).