4-甲基苯胺
外观
4-甲基苯胺 | |
---|---|
别名 | 对甲基苯胺 |
识别 | |
CAS号 | 106-49-0 |
PubChem | 7813 |
性质 | |
化学式 | C7H9N |
摩尔质量 | 107.15 g·mol−1 |
密度 | 1.046 g·cm−3[1] |
熔点 | 44—45 °C(317—318 K)[1] |
沸点 | 200.4 °C(473.5 K)[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
4-甲基苯胺是有机化合物,化学式C₇H₉N,是甲苯胺的同分异构体。
合成
[编辑]4-甲基苯胺可由氢气[2]、水合肼[3]、硼氢化钠[4]、铝汞齐[5]等还原剂还原4-硝基甲苯得到。
反应
[编辑]氨基的反应
[编辑]4-甲基苯胺可以和酰卤或酸酐反应得到相应酰胺,如和对甲苯磺酰氯反应,得到N-(对甲苯基)对甲苯磺酰胺[6];和乙酸酐反应,得到N-对甲基苯基乙酰胺;[7]和酸或卤代烃反应,得到4-甲基苯铵盐或相应的季铵盐;[8]和醛反应,生成氮-碳偶联的产物,如:[9]
苯环的取代反应
[编辑]和N-溴代丁二酰亚胺反应得到2-溴-4-甲基苯胺;[10]碘和二甲基亚砜存在时和4-氟苯硫酚在二甲基甲酰胺反应,可得到取代氨基邻位的产物2-(4-氟苯硫基)-4-甲基苯胺;[11]和甲醛反应生成Tröger氏碱。
参考文献
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- ^ Chen, Min-Hsien; Hsieh, Jen-Chieh; Lee, Yi-Hsien; Cheng, Chien-Hong. Controlled Synthesis of Enantioselective 1-Aminoindenes via Cobalt-Catalyzed [3 + 2] Annulation Reaction. ACS Catalysis. 2018, 8 (10): 9364–9369. ISSN 2155-5435. doi:10.1021/acscatal.8b02566 (英语).
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