Nucleophile Substitutionen an Kohlensäurederivaten. XII. Kinetik und Mechanismus der Reaktion von N‐Nitro‐N‐alkylurethanen mit primären aliphatischen Aminen
Nucleophilic Substitutions to Carbonic Acid Derivates. XII. Kinetics and Mechanism of the Reaction of N‐Nitro‐N‐alkyl‐urethanes with Primary Aliphatic Amines The aminolysis of N‐alkyl‐N‐nitrourethanes takes place, as the kinetical studies demonstrate, by means of several consecutive steps. The nucle...
| Published in: | Journal für Praktische Chemie |
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| Main Authors: | , , , |
| Format: | Article in Journal/Newspaper |
| Language: | English |
| Published: |
Wiley
1980
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| Subjects: | |
| Online Access: | http://dx.doi.org/10.1002/prac.19803220103 http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fprac.19803220103 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fprac.19803220103 https://onlinelibrary.wiley.com/doi/pdf/10.1002/prac.19803220103 |
| Summary: | Nucleophilic Substitutions to Carbonic Acid Derivates. XII. Kinetics and Mechanism of the Reaction of N‐Nitro‐N‐alkyl‐urethanes with Primary Aliphatic Amines The aminolysis of N‐alkyl‐N‐nitrourethanes takes place, as the kinetical studies demonstrate, by means of several consecutive steps. The nucleophilic attack of the amine (first step; reaction B), as well as the proton‐transfere (second step; reaction C), are quick pre‐equilibres, followed by the slow, rate‐determining elimination of the nitramino‐group (reaction D). During the deprotonation, an intermediate with two to the nitramino‐group antiperiplanar orbitals is formed, providing the necessary mesomeric assistance of the elimination. |
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