“…1 H NMR (400 MHz, Chloroform-d) δ (ppm): 7.93 (d, J = 8.8 Hz, 1H), 6.57 (d, J = 8.8 Hz, 1H), 6.36 (s, 1H), 3.44 (q, J = 6.8 Hz, 4H), 2.87 (t, J = 5.6 Hz, 2H), 2.57 (t, J = 6.1 Hz, 2H), 2.10 (p, J = 5.5 Hz, 2H), 1.22 (t, J = 6.9 Hz, 6H). 13 Synthesis of Intermediate II. 3-Hydroxy-N,N-diethylaniline (1.0 g, 6.06 mmol), and CH 2 (COOPh) 2 (1.55 g, 6.06 mmol) were added to anhydrous toluene (20 mL).…”