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Srovnání reaktivity derivátů 1,2,4-dithiazolu při sulfuraci trifenyl-fosfitu
Authors: Hanusek Jiří
Year: 2008
Type of publication: ostatní - přednáška nebo poster
Name of source: Chemické listy
Publisher name: Česká společnost chemická
Place: Praha
Page from-to: nestránkováno
Titles:
Language Name Abstract Keywords
cze Srovnání reaktivity derivátů 1,2,4-dithiazolu při sulfuraci trifenyl-fosfitu V tomto příspěvku je srovnána reaktivita 3-ethoxy-1,2,4-dithiazol-5-onu, 3-methyl-1,2,4-dithiazol-5-onu, 3-fenyl-1,2,4-dithiazol-5-onu, 3-fenyl-1,2,4-dithiazol-5-thionu, 3-amino-1,2,4-dithiazol-5-thionu, 1,2,4-dithiazolidin-3,5-dionu a 4-fenyl-1,2,4-dithiazolidin-3,5-dionu vůči trifenyl-fosfitu v acetonitrilu, dichlormethanu, methanolu a tetrahydrofuranu při 25 °C.
eng Comparison of reactivity of 1,2,4-dithiazole derivatives during sulfurization of triphenyl phosphite In the current study, we have compared reactivity of 3-ethoxy-1,2,4-dithiazole-5-one, 3-methyl-1,2,4-dithiazole-5-one, 3-phenyl-1,2,4-dithiazole-5-one, 3-phenyl-1,2,4-dithiazole-5-thione, 3-amino-1,2,4-dithiazole-5-thione, 1,2,4-dithiazolidine-3,5-dione and 4-phenyl-1,2,4-dithiazolidine-3,5-dione toward triphenyl phosphite in acetonitrile, dichloromethane, methanol and tetrahydrofuran at 25 °C. For 3-ethoxy-1,2,4-dithiazole-5-one we have found that reaction produces very reactive ethoxythiocarbonyl isocyanate which can be trapped by reaction with nucleophiles. 1,2,4-dithiazoles, sulfurization, P(III) compounds, kinetics