“…The resulting mixture was stirred at room temperature for 24 h and was then taken to dryness in vacuo, and the residue was washed with water and diethyl ether successively to afford the yellow crude product, which was further recrystallized in CH 2 Cl 2 / petroleum ether, and the desired yellow crystalline product 2 was obtained in 62% yield (0.078 g). IR (KBr): 3053 m, 2961 w, 2926 w, 1635 w, 1604 s, 1582 s, 1544 m, 1519 s, 1453 s, 1439 s, 1411 s, 1305 m, 1264 m, 1226 m, 1159 m, 1059 m, 1030 m, 1007 m, 964 m, 756 s, 732 m, 697 m, 670 m. 1 H NMR (in CDCl 3 ): δ 2.17 (s, 3H), δ 2.09 (s, 3H), 5.29 (s, 1H), 5.83 (s, 1H), 5.90 (d,J = 8 Hz,2H),6.52 (m,2H),6.72 (m,4H),7.02 (m,2H),7.45 (d,J = 7.6 Hz,2H),3H),7.78 (d,J = 8 Hz,2H),7.85 (d,J = 7.2 Hz,2H),8.88 (d,J = 7.6 Hz,2H). Anal.…”