Abstract
On reaction with N-phenylethyleneimine in the presence of tetraethylammonium bromide, methyl and phenyl isothiocyanates form 2-methyl- and 2-phenyl-imino-3-phenylthiazolidines. In this reaction, methyl isothiocyanate partially trimerizes. Under the action of N-phenylethyleneimine phenylisocyanate trimerizes in high yield.
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