Conclusions
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1.
Thiodiacetone alcohol reacts with the monochlorides of trivalent phosphorus acids in the presence of a base to give tricoordinated phosphorus derivatives. 2-Ethoxy-2-thio-3,5,5-trimethyl-1,2-thia-3-phos-pholanol is formed in the case of ethyl dichlorophosphite.
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2.
The reaction of thiodiacetone alcohol with phenyldichlorophosphine in the absence of a base gives 2-phenyl-2-thio-1,2-oxa-3,3,5-trimethyl-4-phospholene.
Literature cited
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F. M. Rapoport and A. A. Il'inskaya, Laboratory Methods for the Preparation of Pure Gases [in Russian], Goskhimizdat (1963), p. 155.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2121–2124, September, 1974.
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Rizpolozhenskii, N.I., Stepashkina, L.V. & Eliseenkova, R.M. Reaction of thiodiacetone alcohol with chlorides of trivalent phosphorus acids. Russ Chem Bull 23, 2039–2041 (1974). https://doi.org/10.1007/BF00922817
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DOI: https://doi.org/10.1007/BF00922817