化学合成。
化学合成
合成路线 1(1. 合成:22190-35-8)
产率:84%
合成条件:With ethanol; Dimethylphenylsilane; Au-TiO 2 In neat (no solvent) at 70℃; for 3 h;
实验步骤:一般步骤:向含有8-甲氧基喹啉,1(0.048g,0.3mmol),Me2PhSiH(185μL,1.2mmol)和乙醇(70μL,1.2mmol),Au / TiO2(60mg,1.0mol%)的干燥小瓶中加入。 添加。 催化剂中的Au含量为~1wt%。 将混合物加热至70℃并通过TLC和GC监测反应进程。 15分钟后(100%转化),加入乙醇(1mL),并在减压下通过短硅胶垫借助乙醇(2-3mL)过滤得到的浆液,以保留负载的催化剂。 真空蒸发滤液,并将残余物进行色谱分离(正己烷/乙酸乙酯,10:1),得到8-甲氧基-1,2,3,4-四氢喹啉(1a)(41mg,84%收率)。
参考文献:
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合成路线 2(2. 合成:22190-35-8)
产率:35%
合成条件:With N-Bromosuccinimide In tetrachloromethane at 0℃; for 3 h;
实验步骤:将NBS(28g,158mmol)加入到1,2,3,4-四氢喹啉(20g,150.16mmol)的四氯化碳(200mL)溶液中。 将得到的溶液在0℃下搅拌3小时,用二氯甲烷(3×50mL)萃取,真空浓缩,得到残余物,将其用1%乙酸乙酯的石油醚溶液涂于硅胶柱上,得到6 -bromo-1,2,3,4-四氢喹啉,为黄色固体(11g,35%)。LC / MS(ES,m / z):[M + H] + 212.1'H-NMR(300MHz,CDCl3) )δ7.03 - 7.07(m,2H),6.35 - 6.38(m,1H),3.51 - 3.55(m,2H),2.73-2.80(m,2H),1.89 - 1.99(m,2H)
参考文献:
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