Summary
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1.
Some higher α,α,α,ω-tetrachloroalkenes were dehydrochlorinated over zinc chloride, and CCl2 = CH(CH2)9 Cl and CCl2=CH(CH2)11Cl.
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2.
In the dehydrochlorination of 1,1,1,3-tetrachloropropane over zinc chloride a high yield of 1,1,3-trichloropropene is obtained. The same substance may be isolated in the pure state by the dehydrochlorination of 1,1,1,3-tetrachloropropane with caustic alkali when 2-ethoxyethanol is used as solvent.
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A. N. Nesmeyanov, R. Kh. Freidlina, and L. I. Zakharkin, Usp. Khim, 25, 681 (1956).
A. N. Nesmeyanov and L. I. Zakharkin, Izvest, Akad. Nauk SSSR Otdel. Khim. Nauk (1953) 988.
A. N. Nesmeyanov, R. Kh. Freidlina, and V. I. Firstov, Izvest. Akad. Nauk SSSR, Otdel, Khim. Nauk (1951) 505.
British Pat. 581901; C. A. (1947) 2428; British Pat. 2410541, C. A. (1947) 981.
A. N. Nesmeyanov and L. I. Zakharkin, Izvest. Akad. Nauk, Otdel, Khim. Nauk (1955) 224.
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Nesmeyanov, A.N., Semenov, N.A. Preparation of α,α,ω-trichloroalkenes from α,α,α,ω-tetrachloroalkanes. Russ Chem Bull 8, 2022–2024 (1959). https://doi.org/10.1007/BF00909043
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DOI: https://doi.org/10.1007/BF00909043