65039-08-9 1-乙基-3-甲基溴化咪唑
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安全说明
运输方式:冰袋运输。危险性质:非危险化学品。海关编码:29332900,存储类别:11 - 可燃固体,WGK Germany:3。危险性类别:眼部刺激 类别2,经皮刺激 类别2。危险性描述:H315(造成皮肤刺激)、H319(造成严重眼刺激)、H335(可能引起呼吸道刺激)。危险标志:GHS07,信号词:Warning。危险性防范说明:P261(避免吸入粉尘/烟雾)、P305 + P351 + P338(如进入眼睛,立即用大量水冲洗并就医)。
用途与制备
化学合成。
化学合成
产率:98% 合成条件:at 40℃; for 24 h; Schlenk technique; Inert atmosphere 实验步骤:配体(3除外)均通过改进Starikova等人的方法合成。将N-单取代的唑(0.1mmol)和无水甲苯置于双颈烧瓶中并搅拌直至形成均匀的溶液;然后在连续搅拌下滴加烷基卤(0.3mmol)。加入烷基卤化物后,搅拌混合物,同时在40℃加热24小时。除去溶剂,将配体真空干燥。 产物表征:1-甲基-3-乙基咪唑溴化物(2)白色固体,产量(4.70g,98%)。IR(ATR cm -1):3065,2975,1670,1571,1467,1172,1101,856,789,649,789,621,417;δH(400MHz,CDCl3):1.47(3H,t,J 7.3Hz,CH3),3.97(3H,s,NCH3),4.32(2H,q,NCH2),7.54(2H,s,NCH)和10.07ppm(1H,s,CH);δC(100MHz,CDCl3):15.64(CH3),36.63(NCH3),45.18(NCH2),122.01(NCH),123.71(NCH)和136.73ppm;m/z(ESI)111.5(M + -Br-);HRMS(ESI)计算值C6H11BrN2,111.09222(M + -Br-);发现,111.09196(M + -Br-)。 参考文献:[1] Angewandte Chemie - International Edition, 2012, vol. 51, # 46, p. 11483 - 11486 [2] Angew. Chem., 2012, vol. 124, # 46, p. 11650 - 11654,5 [3] Organic and Biomolecular Chemistry, 2013, vol. 11, # 15, p. 2534 - 2542 [4] Journal of Chemical and Engineering Data, 2004, vol. 49, # 4, p. 760 - 764 [5] Patent: WO2006/63656, 2006, A1. 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产率:86% 合成条件:at 20℃; for 2 h; Inert atmosphere 实验步骤:实施例3和4:亚甲基二乙酸酯50mL Schlenk烧瓶配备磁力搅拌棒,在室温下加入EMIM-乙酸酯(20.0g,117.0mmol)和0.5当量二氯甲烷(5.0g,58.7mmol)并进行反应 反应后,在80℃,减压下(85.0%)从反应混合物中蒸馏出纯产物。当二溴甲烷用作底物时,反应在室温下反应快,并且高度放热 。反应通过均相路径进行,纯化产物在80℃减压下从反应混合物中蒸馏出来(产率86.0%)。乙二醇二甲酯:1H NMR(CD3CN,400.13MHz):δ= 2.04(s,6H, CH3),5.64(s,2H,CH2); 13 C NMR:δ= 20.9(CH 3),79.7(CH 2),170.8(CO); FTIR(ATR模式):v = 2996(br),1758(s),1190(s),1009(s),978(s) 参考文献:
产率:90% 合成条件:at 20℃; for 3 h; Inert atmosphere 实验步骤:实施例1和2:乙二醇二乙酸酯;在100mL Schlenk烧瓶上装配磁力搅拌棒,在室温下加入EMIM-乙酸酯(50.0g,0.293mol)和0.5当量的1,2-二氯乙烷(14.5g,0.146mol)并在70°C,3小时。反应后,得到两相,倾析上层,反应混合物用乙醚萃取3次,合并所有馏分,真空除去乙醚。得到最终的纯产物,为无色液体(90.0%收率)。当使用1,2-二溴乙烷作为底物时,即使在室温下反应也非常快并且是高度放热的。反应通过均相途径进行;在100℃减压下从反应混合物中蒸馏出纯产物(90.0%收率)。乙二醇二乙酸酯:1 H NMR(CDCl 3,400.13MHz):δ= 2.02(s,6H,CH 3),4.2(s,4H,CH 2); 13 C NMR:δ= 20.9(CH 3),62.3(CH 2),170.9(CO); FTIR(ATR模式):v = 2961(br),1735(s),1371(m),1213(s),1048(m)。 参考文献: