Abstract
(2-Alkoxy-3-phenylpropyl)trichlorotellanes were synthesized by regioselective reaction of tellurium tetrachloride with allylbenzene in the system MeOH–CH2Cl2, as well as by nucleophilic substitution of chlorine in trichloro(2-chloro-3-phenylpropyl)tellane in MeOH–CH2Cl2 and EtOH–CHCl3. Allylbenzene reacted with tellurium tetrabromide on heating in methanol or ethanol. The reduction of (2-alkoxy-3-phenylpropyl) trihalotellanes with NaBH4 in H2O–THF gave 1,2-bis(2-alkoxy-3-phenylpropyl)ditellanes.
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Original Russian Text © M.V. Musalova, M.V. Musalov, S.I. Udalova, A.G. Khabibulina, A.I. Albanov, V.A. Potapov, S.V. Amosova, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 4, pp. 528–531.
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Musalova, M.V., Musalov, M.V., Udalova, S.I. et al. Alkoxytelluration of Allylbenzene. Russ J Org Chem 54, 526–529 (2018). https://doi.org/10.1134/S1070428018040024
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DOI: https://doi.org/10.1134/S1070428018040024