Alkoxytelluration of Allylbenzene


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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.

About the authors

M. V. Musalova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

M. V. Musalov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

S. I. Udalova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

A. G. Khabibulina

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

A. I. Albanov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

V. A. Potapov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

S. V. Amosova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Author for correspondence.
Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

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