One-Step Synthesis of a Silicon-substituted Norbornene Derivative Using the Bis-Silylation Reaction of Norbornadiene-2,5 with 1,1,1,2,2,2-Hexamethyldisilane

The possibility of a one-step synthesis of a norbornene derivative with two organosilicon substituents via the bis-silylation reaction of norbornadiene-2,5 (NBD) with 1,1,1,2,2,2-hexamethyldisilane was investigated. As a result, 5,6-bis(trimethylsilyl)norbornene-2 (BTSNTC) was obtained with high yield and high selectivity in the presence of a palladium catalyst and an isocyanide ligand. A significant influence of the solvent nature and the introduction of basic additives on the reaction rate and the maximum achievable NBD conversions was demonstrated. The optimal solvents and additives are toluene, 1,4-dioxane, and potassium tert-butoxide, respectively.

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Publication Details

Journal
Russian Journal of Applied Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s1070427225120018
Primary Topic
Organoboron and organosilicon chemistry
Type
article
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article

One-Step Synthesis of a Silicon-substituted Norbornene Derivative Using the Bis-Silylation Reaction of Norbornadiene-2,5 with 1,1,1,2,2,2-Hexamethyldisilane

P. P. Lezhnin, M. V. Bermeshev
Russian Journal of Applied Chemistry
Organoboron and organosilicon chemistry
article

One-Step Synthesis of a Silicon-substituted Norbornene Derivative Using the Bis-Silylation Reaction of Norbornadiene-2,5 with 1,1,1,2,2,2-Hexamethyldisilane

P. P. Lezhnin, M. V. Bermeshev
article en

Abstract

The possibility of a one-step synthesis of a norbornene derivative with two organosilicon substituents via the bis-silylation reaction of norbornadiene-2,5 (NBD) with 1,1,1,2,2,2-hexamethyldisilane was investigated. As a result, 5,6-bis(trimethylsilyl)norbornene-2 (BTSNTC) was obtained with high yield and high selectivity in the presence of a palladium catalyst and an isocyanide ligand. A significant influence of the solvent nature and the introduction of basic additives on the reaction rate and the maximum achievable NBD conversions was demonstrated. The optimal solvents and additives are toluene, 1,4-dioxane, and potassium tert-butoxide, respectively.

Russian Journal of Applied ChemistryVol. 98(12)
Russian Academy of Sciences (RU), A.V. Topchiev Institute of Petrochemical Synthesis (RU), Institute of Synthetic Polymeric Materials (RU)
Openalex Percentile: Top 31%
Organoboron and organosilicon chemistry
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