Beilstein Journal of Organic Chemistry (Mar 2016)

Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes

  • Vladimir A. D’yakonov,
  • Alevtina L. Makhamatkhanova,
  • Rina A. Agliullina,
  • Leisan K. Dilmukhametova,
  • Tat’yana V. Tyumkina,
  • Usein M. Dzhemilev

DOI
https://doi.org/10.3762/bjoc.12.43
Journal volume & issue
Vol. 12, no. 1
pp. 406 – 412

Abstract

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An efficient one-pot process for the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes was developed. The method involves the replacement of aluminium in aluminacyclopentanes, prepared in situ by catalytic cycloalumination of α-olefins and α,ω-diolefins, by phosphorus atoms on treatment with dichlorophosphines (R′PCl2). Hydrogen peroxide oxidation and treatment with S8 of the synthesized phospholanes and α,ω-bisphospholanes afforded the corresponding 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-oxides, 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-sulfides, bisphospholane 1,1'-dioxides, and bisphospholane 1,1'-disulfides in nearly quantitative yields. The complexes LMo(CO)5 (L = 3-hexyl-1-phenylphospholane, 3-benzyl-1-methylphospholane, 1,2-bis(1-phenylphospholan-3-yl)ethane, and 1,6-bis(1-phenylphospholan-3-yl)hexane were prepared by the reaction of 3-substituted phospholanes and α,ω-bisphospholanes with molybdenum hexacarbonyl. The structure of the complexes was proved by multinuclear 1H, 13C, and 31P spectroscopy.

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