706791-83-5

基本信息
3-溴-5-胺基苯甲酸甲酯
3-氨基-5-溴苯甲酸甲酯
3-氨基-5-溴苯甲酸甲酯甲酯
Methyl 3-Amino-5-bromobenzoate
Benzoic acid, 3-amino-5-bromo-, methyl ester
物理化学性质
制备方法

6307-87-5

706791-83-5
以3-溴-5-硝基苯甲酸甲酯(51)(1.79 g,6.86 mmol,1当量)为原料,与铁粉(2.3 g,41.2 mmol,6当量)在甲醇(40 mL)中悬浮,缓慢滴加6N盐酸(28 mL)。反应混合物在回流条件下搅拌45分钟。反应完成后,冷却至室温,用水(150 mL)稀释,并用碳酸氢钠中和。所得绿棕色溶液用氯仿萃取四次。合并有机相,用硫酸钠干燥,减压浓缩,得到标题化合物3-氨基-5-溴苯甲酸甲酯(52),为浅黄色固体(1.45 g,6.3 mmol,收率92%)。薄层色谱(硅胶60,氯仿/甲醇 95:5)Rf = 0.56。熔点为190.8℃。1H NMR(300 MHz,CDCl3)δ: 8.14(s,1H,NH2),7.57(dd,1H,4JH-H = 1.6 Hz,Ar-CH-2),7.54(dd,1H,4JH-H = 1.7 Hz,Ar-CH-6),7.42(dd,1H,4JH-H = 1.7 Hz,Ar-CH-4),3.84(s,3H,COOCH3)。13C NMR(75 MHz,CDCl3)δ: 164.8(Ar-COOMe),143.0(Ar-C-NH2),132.4(Ar-C-1),125.0(Ar-CH-4),124.3(Ar-CH-2),122.1(Ar-C-Br),118.1(Ar-CH-6),52.6(OCH3)。IR(ATR)νmax: 3067(w),2952(w),2839(m),2583(w),1730(s),1536(m),1439(m),1428(m),1290(s),1210(s),1113(m),976(m),914(w),881(m),830(m),766(s),731(m),662(m)cm-1。EI-MS(EI+,70 eV)m/z: 229/231(100)[M]+, 198/200(48),170/172(30),171/173(35),143/154(5),90/92(15),63(26)。HRMS(ESI-)计算值C8H9N79BrO2 [M + H]+: 229.9811,实测值: 229.9819 amu。
参考文献:
[1] Tetrahedron, 2010, vol. 66, # 42, p. 8254 - 8260
[2] Patent: WO2004/50619, 2004, A1. Location in patent: Page 21
[3] Chirality, 2015, vol. 27, # 8, p. 487 - 491
[4] Journal of the American Chemical Society, 2013, vol. 135, # 46, p. 17408 - 17416
[5] Patent: WO2014/19685, 2014, A1. Location in patent: Page/Page column 13; 39; 40