Synthesis of Trans-3,4-Dibenzyl-2-Oxo-Tetrahydrofuran: Advanced Study
Theory and Applications of Chemistry Vol. 4,
Page 64-68
Abstract
Trans-3,4-dibenzyl-2-oxo-tetrahydrofuran (6) a substituted tetrahydrofuranoid lignan was synthesized in 70% yield via the Stobbe condensation between (1) benzaldehyde and (2) diethyl succinate. The structure was confirmed by the spectral data such as infra-red, proton magnetic resonance and mass spectrum. It has two similar but non equivalent aromatic groups which appeared at δ: 6.48 - 6.76 and 7.06-7.25 as multiplets.
Keywords:
- Lignans
- tetrahydrofuranoid
- stobbe
How to Cite
Jack, I. R., & Orubite, K. O. (2020). Synthesis of Trans-3,4-Dibenzyl-2-Oxo-Tetrahydrofuran: Advanced Study. Theory and Applications of Chemistry Vol. 4, 64-68. Retrieved from https://stm1.bookpi.org/index.php/tac-v4/article/view/1099
- Abstract View: 0 times