“…The product was extracted three times with diethyl ether (1 × 400 mL, 2 × 300 mL). The organic phase was washed with brine three times (1 × 300 mL, 2 × 200 mL) and dried over anhydrous MgSO 4 , and the solvent was evaporated under vacuum to yield a light yellow oil (24.1 g, 88.0%) 1. H NMR (CDCl 3 , 300 MHz): δ (ppm) 6.95−6.76 (m, 3H, H Ar ), 6.63 (dd, J = 10.9, 17.6 Hz, 1H, Ph-CH� CH 2 ), 5.59 (d, J = 17.6 Hz, 1H, Ph-CH�CH 2 ), 5.12 (d, J = 10.8, 1H, Ph-CH�CH 2 ), 3.90−3.82 (m, 6H, −OCH 3 ) 13.…”