二甲基硫代甲酰胺
外观
二甲基硫代甲酰胺 | |
---|---|
识别 | |
CAS号 | 758-16-7 |
性质 | |
化学式 | C3H7NS |
摩尔质量 | 89.16 g·mol−1 |
外观 | 淡黄色油状液体 |
密度 | 1.047 g·cm−3(0 °C)[1] |
沸点 | 96.5—97 °C(369.6—370.1 K)(12 mmHg) 227—228 °C(500—501 K)[1] |
溶解性(水) | 可溶于冷水,和热水混溶; 可溶于苯、氯仿; 难溶于石油醚[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
二甲基硫代甲酰胺是一种硫代酰胺,化学式为C3H7NS,它是味苦且有强烈气味的淡黄色油状液体。[1]它可由二甲基甲酰胺和五硫化二磷[2]或劳森试剂[3]反应得到。它和三乙基硅基(羰基)(η5-环戊二烯基)(吡啶)合铁在苯中于室温反应,可以得到三乙基硅硫基(羰基)(二甲氨基亚甲基)(η5-环戊二烯基)合铁。[4]它和甲基苯基亚砜在酸存在下反应,可以得到苯甲硫醚。[5]
参考文献
[编辑]- ^ 1.0 1.1 1.2 1.3 Richard Willstätter, Theodor Wirth. Über Thioformamid. Berichte der deutschen chemischen Gesellschaft. 1909-04, 42 (2): 1908–1922 [2022-06-18]. ISSN 0365-9496. doi:10.1002/cber.19090420267 (英语).
- ^ Thomas J. Curphey. Thionation with the Reagent Combination of Phosphorus Pentasulfide and Hexamethyldisiloxane. The Journal of Organic Chemistry. 2002-09-01, 67 (18): 6461–6473 [2022-06-18]. ISSN 0022-3263. doi:10.1021/jo0256742. (原始内容存档于2022-06-21) (英语). (页面存档备份,存于互联网档案馆)
- ^ Rajender S. Varma, Dalip Kumar. Microwave-Accelerated Solvent-Free Synthesis of Thioketones, Thiolactones, Thioamides, Thionoesters, and Thioflavonoids. Organic Letters. 1999-09-01, 1 (5): 697–700 [2022-06-18]. ISSN 1523-7060. doi:10.1021/ol990629a. (原始内容存档于2019-07-19) (英语). (页面存档备份,存于互联网档案馆)
- ^ Kozo Fukumoto, Akane Sakai, Tsukuru Oya, Hiroshi Nakazawa. Desulfurization of N,N-dimethylthioformamide by hydrosilane with the help of an iron complex. Isolation and characterization of an iron–carbene complex as an intermediate of CS double bond cleavage. Chemical Communications. 2012, 48 (32): 3809 [2022-06-18]. ISSN 1359-7345. doi:10.1039/c2cc17163e (英语).
- ^ Haruo Kamijo, Toshio Takido, Toshikatsu Nakazawa, Kunio Itabashi, Manabu Seno. A NOVEL METHOD OF SULFIDE SYNTHESIS FROM SULFOXIDES WITH N,N -DIMETHYLTHIOFORMAMIDE. Phosphorus, Sulfur, and Silicon and the Related Elements. 1993-02, 82 (1-4): 207–210 [2022-06-18]. ISSN 1042-6507. doi:10.1080/10426509308047423 (英语).