Summary
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1.
It has been shown for the first time that reduction by means of lithium hydride can be successfully extended to alkyihalosilanes and other classes of organosilicon compounds (alkenylhalosilanes, halo(haloalkyl)silanes, alkylethoxy-silanes), and in the last case reduction proceeds selectively, without affecting the halogen of the haloalkyl group.
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2.
It has been shown that diallylsilane undergoes thiocyanation in almost theoretical yield, and that allylsilane combines with HCl in accordance with Markovnikov's rule.
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3.
The results provide data that characterize the dependence -of the freezing points of some silanes on their structure. It has been shown also that the value of the refraction fof the Si-C bond is determined by the radical containing the carbon attached to silicon, In particular, for allyl attached to silicon this value should be taken as 2.68 ml/mole.
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Ponomarenko, V.A., Mironov, V.F. Synthesis of some alkenyl- and alkyl-silanes and their derivatives. Russ Chem Bull 3, 423–427 (1954). https://doi.org/10.1007/BF01167820
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DOI: https://doi.org/10.1007/BF01167820