8-bromo-6-tert-butylquinoline 化学特性,用途語,生産方法
製造方法
2-Bromo-4-tert-butylaniline (7.41 g, 32.5 mmol), phloroglucinol (1.07 g, 8.5 mmol) and hydrochloric acid (37%, 0.5 mL) were added in a 100 mL flask. The flask was heated in an oil bath at 120℃ for 4 hours. After cooling down to room temperature, ethanol (20 mL) was added to the flask and the solid was crashed. The suspension was filter off and the solid was further washed with ethanol (40 mL) to give 8-bromo-6-tert-butylquinoline as colourless powder (5.46 g, 7.2 mmol, 85%). m.p. 230℃.
1H NMR (600 MHz, DMSO-d6) δ (ppm) = 7.50 (d, J = 2.2 Hz, 3H), 7.30 (dd, J = 8.5, 2.2 Hz, 3H), 7.26 (d, J = 8.5 Hz, 3H), 7.22 (s, 3H), 6.12 (s, 3H), 1.24 (s, 27H). 13C NMR (150 MHz, DMSO-d6) δ (ppm) =145.53, 145.35, 138.67, 129.53, 125.09, 121.56, 115.34, 97.60, 33.96, 31.03. IR (KBr) ? (cm-1 ) = 3397, 2962, 2903, 2867, 1597, 1512, 1491, 1389, 1362, 1307, 1266, 1176, 1117, 1041, 876, 855, 816, 731, 690, 599, 421. HRMS (ESI) (m/z): [M+H] + calculated. for C36H43N3Br3, 754.1007; found, 754.1005
8-bromo-6-tert-butylquinoline 上流と下流の製品情報
原材料
準備製品