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Poppe

In 1889, Popp (104) confirmed the structure of 2-aminothiazole (72) by diazotization and reduction he obtained thiazole itself (73). [Pg.24]

Probably first obtained by Hantzsch and Arapides (105) by condensation of a,/3-dichlorether with barium thiocyanate, and identified by its pyridine-like odor, thiazole was first prepared in 1889 by G. Popp (104) with a yield of 10% by the reduction in boiling ethanol of thiazol-2-yldiazonium sulfate resulting from the diazotization of 2-aminothiazole. prepared the year before by Traumann (103). The unique cyclization reaction affording directly the thiazole molecule was described in 1914 by Gabriel and Bachstez (106). They applied the method of cyclization, developed by Gabriel (107, 108), to the diethylacetal of 2-formylamino-ethanal and obtained thiazole with a yield of 62% - Thiazole was also formed in the course of a study on the ease of decarboxylation of the three possible monocarboxylic acids derived from it (109). On the other... [Pg.24]


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See also in sourсe #XX -- [ Pg.267 ]




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H. Poppe)

Popp, F D„ Moynahan, E. B., Heterocyclic

Popp, F D„ Moynahan, E. B., Heterocyclic Ferrocenes

Popp, F. D., Catala Noble, A., The Chemistry of Diazepines

Popp, F. D., Developments in the Chemistry of Reissert Compounds

Popp, F. D„ Catala Noble, A., The Chemistry

Popp, F. D„ Developments in the Chemistry

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