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چکیده
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In this study, the one-pot reaction of maleic anhydride with a
combination of aromatic and aliphatic thiols, or with an alcohol
and thiol mixture, in the presence of triphenylphosphine catalyst
has been investigated. The reaction with the mixture of thiols
occurs in a single step, and despite the presence of two different
thiols in the reaction medium, a unique product is formed. The
aromatic thiol facilitates the ring-opening of the anhydride, while
the aliphatic thiol participates solely in the Michael addition to
the intermediate. When a mixture of alcohol and thiol is used
in the medium, the reaction proceeds in two steps. In this reac
tion, the alcohol opens the anhydride ring, and the thiol induces
nucleophilic addition to the acrylate intermediate.
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