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2-Methyl-tetrahydrofuran-3-thiol

A thio-substituted, quaternary ammonium salt can be synthesized by the Michael addition of an alkyl thiol to acrylamide in the presence of benzyl trimethyl ammonium hydroxide as a catalyst [793-795]. The reaction leads to the crystallization of the adducts in essentially quantitative yield. Reduction of the amides by lithium aluminum hydride in tetrahydrofuran solution produces the desired amines, which are converted to desired halide by reaction of the methyl iodide with the amines. The inhibitor is useful in controlling corrosion such as that caused by CO2 and H2S. [Pg.92]


See other pages where 2-Methyl-tetrahydrofuran-3-thiol is mentioned: [Pg.344]    [Pg.23]    [Pg.149]    [Pg.80]    [Pg.621]    [Pg.202]    [Pg.202]    [Pg.80]    [Pg.902]    [Pg.159]    [Pg.1745]   
See also in sourсe #XX -- [ Pg.207 ]




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