Reaktion #306975
ord-23b1e941530343dbbed218007f52dd70
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1EinengenThe reaction mixture was concentrated
- 2Sonstigeto give a brown solid which
- 3Waschenthe aqueous phase was washed twice with EtOAc
- 4Einengenit was concentrated until precipitation (half of the volume)
- 5FiltrationThe suspension was filtered
Vorschrift
A solution of methyl 2′-methyl-2-(trifluoromethyl)biphenyl-4-carboxylate (5 g; 16.99 mmol; 1 eq.) in EtOH (150 mL) at RT was treated with sodium hydroxide (10.19 mL; 5 M; 50.97 mmol; 3 eq.). The reaction mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated to give a brown solid which was taken up in water (300 mL) and the aqueous phase was washed twice with EtOAc. The aqueous phase was acidified with HCl cc to pH 2, then it was concentrated until precipitation (half of the volume). The suspension was filtered affording the title compound as a beige solid. 1H NMR (DMSO-d6, 300 MHz) δ 13.55 (br s, 1H), 8.31 (s, 1H), 8.26-8.23 (d, J=7.90 Hz, 1H), 7.51-7.48 (d, J=7.90 Hz 1H), 7.37-7.12 (m, 4H), 1.99 (s, 3H). LC/MS (Method A): 278.9 (M−H)−. HPLC (Method A) Rt 4.57 min (Purity: 98.7%).