1043-50-1Relevant articles and documents
Chambers,Cunningham
, p. 469 (1966)
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Deacon,Parrott
, p. P17 (1969)
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Cohen et al.
, p. 451 (1967)
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Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
Makarov, Alexander Yu.,Bagryanskaya, Irina Yu.,Zhivonitko, Vladimir V.
, (2020)
[Figure not available: see fulltext.] Reactions of 1,3λ4δ2,2,4-benzothiadiazines with SCl2, C6F5SCl, and [NS2][SbF6] leading to 1,2,3-benzodithiazolium salts (Herz salts) were in
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Clark, R. J. H.,Kaminaris, D.
, p. L7 - L8 (1974)
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Convenient Synthesis of Symmetrical Polyfluorinated Diphenyl Sulfides
Bredikhin, R. A.,Maksimov, A. M.,Nikul’shin, P. V.,Platonov, V. E.
, p. 1921 - 1930 (2022/01/24)
Abstract: Thermal properties of decafluorodiphenyl disulfide in the pure state and in the presence of copper and iron metals have been studied. A procedure has been proposed for the synthesis of symmetrical poly-fluorinated diaryl sulfides from diaryl dis
HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXVII. REACTIONS OF ALKANETHIONES WITH THE CHLORINE DERIVATIVES OF BENZENE, THIOPHENE, AND NAPHTHALENE
Voronkov, M. G.,Deryagina, E. N.,Sukhomazova, E. N.
, p. 755 - 760 (2007/10/02)
Alkanethiols react effectively with chlorobenzene, its derivatives, 1-chloronaphthalene, and 2-chlorothiophene at 600-660 deg C with the preferential formation of the corresponding aromatic or heteroatomic thiols.Ethanethiol is most reactive.When it is used instead of hydrogen sulfide in reactions with chlorobenzene or its 4-substituted derivatives, the yield of the aromatic thiols, from which the phenylthiyl radicals are generated with greater difficulty, increases more sharply than the yield of the thiophenols, which generate the more stable 4-XC6H4S radicals.The side products of the reactions are the corresponding diaryl sulfides, thiophene, benzothiophene, and toluene.