N-乙酰基乙酰苯胺
| N-乙酰基乙酰苯胺 | |
|---|---|
| |
| 别名 | N,N-二乙酰基苯胺 |
| 识别 | |
| CAS号 | 1563-87-7 
|
| 性质 | |
| 化学式 | C10H11NO2 |
| 摩尔质量 | 177.2 g·mol−1 |
| 熔点 | 37.5 °C（310.6 K）[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
N-乙酰基乙酰苯胺是一种有机化合物，化学式为C10H11NO2。它可由乙酰苯胺和乙酰氯[2]或乙酸酐[3]反应得到。它和劳森试剂反应，可以得到硫代乙酰苯胺。[4]它可以在HCl中重排，得到4-氨基苯乙酮。[5]
参考文献
[编辑]- ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-10-11].
- ^ Heyns, Kurt; Pyrus, Wolfgang. Reactions of the carbonamide group. III. Reaction with organometallic compounds. Chemische Berichte, 1955. 88: 678-683.
- ^ Nagaraj R. Ayyangar, Kumar V. Srinivasan. Effect of substituents in the formation of diacetanilides. Canadian Journal of Chemistry. 1984-07-01, 62 (7): 1292–1296 [2021-10-11]. ISSN 0008-4042. doi:10.1139/v84-215 （英语）.
- ^ Meyer, H. J.; Nolde, C.; Thomsen, I.; Lawesson, S. O. Preparation and some reactions of N,N-diacetylamines. Bulletin des Societes Chimiques Belges, 1978. 87 (8): 621-626.
- ^ J. F. J. Dippy, V. Moss. 411. The rearrangement of NN-diacylanilnes and the nuclear benzoylation of anilines. Journal of the Chemical Society (Resumed). 1952: 2205 [2021-10-11]. ISSN 0368-1769. doi:10.1039/jr9520002205 （英语）.