Synthesis of New Heterocyclic Compounds Using Lawesson Reagent
Lawesson reagent 1 reacts with Mannich bases of -naphthol 2 and 8 -hydroxyquinoline 4 to give oxthiaphosphinine- 3 -sulfide derivatives 3 and 5, respectively. Reaction of 1 with benzaldehyde in the presence of trialkyl phosphite yields 1,3,5,2-trithiaphosphinane-2-sulfide derivative 8 and, in the presence of ethyl acrylate, affords 2,4,6-triphenyl-1,3,5-trithiane 9. A mechanism is proposed to explain the formation of adduct 3.
Keywords: Lawesson reagent; Mannich bases; benzaldehyde; ethyl acrylate; trialkyl phosphite
Document Type: Research Article
Affiliations: Department of Pesticide Chemistry, National Research Centre, Dokki, Cairo, Egypt
Publication date: 01 February 2006
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