Zur Kenntnis der Reaktionsfähigkeit des Thiomorpholins und alkylsubstituierter Thiomorpholine, 4. Mitt. |
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| Authors: | Friedrich Asinger Alfons Saus Magdalena von Wachtendonk |
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| Affiliation: | (1) Institut für Technische Chemie und Petrolchemie, Rheinisch-Westfälische Technische Hochschule, Aachen, Bundesrepublik Deutschland;(2) Present address: FB6 (Angewandte Chemie), Gesamthochschule Duisburg, Postfach 10 16 29, D-4100 Duisburg 1, Bundesrepublik Deutschland |
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| Abstract: | Thiomorpholine as well as alkyl substituted thiomorpholines and their Sdioxides, respectively, are transformed into the corresponding N-Aminothiomorpholines by nitrosation (1–5) followed by the reduction with zinc in acetic acid/acetic acid anhydride under simultaneous formation of the corresponding N-acetyl derivates, and hydrolysis by hydrochloric acid (6–9). Examples of this method are described. 4-Aminothiomorpholines and their Sdioxides react with aldehydes or ketones to give azomethines (10–31). Acylation with mono-and dicarbonic acid chlorides leads to the N-acyl derivatives32–44.Mannich condensation is also possible. By oxidation with yellow mercury oxide tetracenes are formed (46–47).Teil der DissertationM. Schmitz, Techn. Hochschule Aachen, 1975. |
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| Keywords: | N-Acylamino-thiomorpholines N-Amino-thiomorpholines N-Nitroso-thiomorpholines Tetracenes Thiomorpholines |
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