A simple one-pot synthesis of phosphinoselenoic amides and diamides from secondary phosphine selenides and amines using Et3N-CCl4

Tetrahedron Letters

Volumn 52, Issue 18, 2011, Pages 2367-2369

  Gusarova, Nina K ^a   Volkov, Pavel A ^a   Ivanova, Nina I ^a   Larina, Ludmila I ^a   Trofimov, Boris A ^a  

^a A E FAVORSKY IRKUTSK INSTITUTE OF CHEMISTRY   (Russian Federation)

Author keywords

Amines; Phosphinoselenoic amides; Secondary phosphine selenides

Indexed keywords

AMIDE; AMINE; CARBON TETRACHLORIDE; DIAMIDE; SELENIDE;

ARTICLE; CHEMICAL REACTION; ONE POT SYNTHESIS;

EID: 79953282776     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.02.095     Document Type: Article

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32. 4 (1 ml) was added, and the mixture was stirred at 20-25 °C for 50 min. The solvent was removed under reduced pressure, and 1,4-dioxane (3 ml) was added. The precipitated white solid (triethylammonium chloride) was removed by filtration and the 1,4-dioxane evaporated under vacuum. The residue obtained was washed with hot hexane (2 × 3 ml), and the hexane solution was allowed to stand for 12 h at 0-1 °C. The hexane layer was filtered and evaporated under vacuum. The residue was dried in vacuo to give amides 8a-f.
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34. 4 (1 ml) was added, and the reaction mixture stirred at 20-25 °C for 50 min. The solvent was removed under reduced pressure, and 1,4-dioxane (3 ml) was added. The precipitated white solid (triethylammonium chloride) was removed by filtration and the 1,4-dioxane evaporated under vacuum. The crude product was washed with hot hexane (3 × 2 ml), and the hexane was removed by decanting. The residue was dried under vacuo to give diamides 13a-e.