“…4-Isopropyl-2-methylpyridine was prepared according to the method of Comins and Abdullah (1982) in 52% yield. The spectral data were as follows: RI = 1059; IR (film) 3080, 3030, 2975,1603,1560,920,830 cm"1; NMR (CDC13) 1.20 (d, «7 = 7 Hz, 6 H, two CH3), 2.47 (s, 3 H, CH3), 2.79 (dq, «7=7 and 7 Hz, 1H, CH), 6.84 (d, «7 = 5 Hz, , H), 6.87 (s, , H), 8.25 (d, «7 = 5 Hz, 1H, Ar H); EI-MS m/z (relative intensity) 135 (M+, 64), 120 (100), 106 (4), 93 (6), 77 (13), 65 (5), 42 (6), 41 (6). 3-Phenyl-4-propylpyridine was prepared from 3-phenylpyridine and butyric acid according to the modified method of Minisci et al (1971), and it showed the same physicochemical properties as those reported by Sakurai et al (1983).…”