1,2-二碘乙烷是一种有机化合物,化学式为C2H4I2。
1,2-二碘乙烷可由乙烯和碘单质反应得到:[3]
- C2H4 + I2 ⇌ C2H4I2
1,2-二氯乙烷和碘化钠在四丁基碘化铵的催化下于DMF中加热,发生卤素交换反应,得到1,2-二碘乙烷。[4]乙二醇和氢碘酸加热反应,也可得到该化合物。[5]
1,2-二碘乙烷在有机合成中主要用于二碘化钐和二碘化镱的制备:[6]
- Sm + ICH2CH2I → SmI2 + H2C=CH2 (惰性气氛、THF作为溶剂)
- ^ 1.0 1.1 Jaeger, F. M. Crystallography of the Aliphatic Compounds. Zeitschrift fuer Kristallographie und Mineralogie, 1909. 45: 539-547. ISSN: 0372-9176.
- ^ Gordon G. Cash, Suzanne Hartigan, Jay Tunkel. Normal boiling points of haloalkanes from electrotopological state indices. Toxicological & Environmental Chemistry. 2008-11, 90 (6): 1073–1089 [2020-05-29]. ISSN 0277-2248. doi:10.1080/02772240701862116 (英语).
- ^ Cutherbertson, G.R.; Kistiakowsky, G.B. The thermal equilibrium between ethylene iodide, ethylene and iodine. J. Chem. Phys. 1935, 3 (10): 631–634. Bibcode:1935JChPh...3..631C. doi:10.1063/1.1749566.
- ^ Herlekar, Omkar Pravin; Durve, Ketakee Sanjay; Chaudhari, Nikhil Vitthal. Process for terminal dihaloalkane. 2012. IN 2012MU01684 A.
- ^ Doya, Masaharu; Hoshino, Yuki. Preparation of iodine compounds by alcohol iodination using hydriodic acid while removing generated water. 2010. JP 2010159223 A.
- ^ Girard, P.; Namy, J. L.; Kagan, H. B. Divalent lanthanide derivatives in organic synthesis. 1. Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agents. Journal of the American Chemical Society. 1980, 102 (8): 2693–2698. doi:10.1021/ja00528a029.
卤代乙烷 |
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| 單鹵代 | |
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| 雙鹵代 | |
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| 三鹵代 | |
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| 四鹵代 | |
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| 五鹵代 | |
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| 六鹵代 | |
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| *:有手性的化合物 // χ:尚未被发现的化合物 |
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