Summary
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1.
Triethylphosphonamidous hloride and alkyl triethylphosphonatnldites (ranging from the methyl to the decyl ester) were synthesized.
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2.
Triethylphosphoamidothloic chloride was prepared by addition of sulfur to triethylphosphonamidous chloride in presence of aluminum chloride.
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3.
Alkyl triethylphosphonamidothicate, (ranging from the methyl to the decyl ester) were ptepared by addition of sulfur to alkyl triethylphosphonamidites.
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4.
When trlethylphosphonamldous chloride was treated with as alcohol. the arnido group was eliminated In the form of diethylamine hydrochloride and a dialkyl ethylphosphonite was formed.
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Literature cited
G. M. Koslapoff and R. M Watson. J. Am. Chem. Soc., No. 9, 73,4101 (1953).
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Arbuzov, B.A., Rizpolcabearky, H.I. & Zvereva, M.A. Esters of ethylphosphonous acid, and some of their reactions. Russ Chem Bull 4, 935–943 (1955). https://doi.org/10.1007/BF01172113
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DOI: https://doi.org/10.1007/BF01172113