α-硝基甲苯
| α-硝基甲苯 | |
|---|---|
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| 英文名 | α-nitrotoluene (nitromethyl)benzene |
| 識別 | |
| CAS號 | 622-42-4 
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| SMILES |
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| 性質 | |
| 化學式 | C7H7NO2 |
| 摩爾質量 | 137.14 g·mol−1 |
| 熔點 | 80.7 °C（353.8 K）[1] |
| 沸點 | 114—115 °C（387—388 K）（12 Torr）[2] 231—233 °C（504—506 K）（分解）[3] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
α-硝基甲苯是一種有機化合物，化學式為C7H7NO2。它可由亞硝酸銀和溴化苄在乙醚中反應得到。[4]苯甲醇和亞硝酸鈉在乙酸的存在下於二氯甲烷中反應，也能製得α-硝基甲苯。[5]它可以被還原劑還原為苄胺。[6]
參考文獻
- ^ Copisarow, M. The purification of trinitrotoluene. Chemical News and Journal of Industrial Science, 1916. 113. 37-38.
- ^ Zalukajevs, L. Preparation of phenylnitromethane from phenylacetic acid（俄文）. Latvijas PSR Zinatnu Akademijas Vestis, 1954. 3/80. 101-106.
- ^ G. B. Brown, R. L. Shriner. SALTS OF NITRO COMPOUNDS. II. THE REACTION OF THE SILVER SALT OF PHENYLNITROMETHANE WITH DIPHENYLBROMOMETHANE. The Journal of Organic Chemistry. 1937-09, 02 (4): 376–380 [2020-06-27]. ISSN 0022-3263. doi:10.1021/jo01227a010 （英語）.
- ^ Guofei Huang, Xiaoyu Ren, Chunhui Jiang, Jia-Hong Wu, Guowei Gao, Tianli Wang. Efficient synthesis of ( E )-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement. Organic Chemistry Frontiers. 2019, 6 (16): 2872–2876 [2020-06-27]. ISSN 2052-4129. doi:10.1039/C9QO00478E （英語）.
- ^ A. Vidal-Albalat, K. Świderek, J. Izquierdo, S. Rodríguez, V. Moliner, F. V. González. Catalytic enantioselective epoxidation of nitroalkenes. Chemical Communications. 2016, 52 (65): 10060–10063 [2020-06-27]. ISSN 1359-7345. doi:10.1039/C6CC03539F （英語）.
- ^ Lei Yu, Qi Zhang, Shu-Shuang Li, Jun Huang, Yong-Mei Liu, He-Yong He, Yong Cao. Gold-Catalyzed Reductive Transformation of Nitro Compounds Using Formic Acid: Mild, Efficient, and Versatile. ChemSusChem. 2015-09-21, 8 (18): 3029–3035 [2020-06-27]. doi:10.1002/cssc.201500869 （英語）.