Bohn–Schmidt Reaction
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Bohn–Schmidt Reaction
The Bohn–Schmidt reaction, a named reaction in chemistry, introduces a hydroxy group at an anthraquinone system. The anthraquinone must already have at least one hydroxy group. The reaction was first described in 1889 by René Bohn (1862–1922) and in 1891 by Robert Emanuel Schmidt (1864–1938), two German industrial chemists. René Bohn is one of the few industrial chemists after whom a reaction is named. In 1901, he made indanthrone from 2-aminoanthraquinone and thus laid the basis for a new group of dyes. Reaction mechanism The postulated reaction mechanism is explained below for the example of 2-hydroxyanthraquinone: The sulfuric acid protonates the keto group of the anthraquinone 1. This causes a shift of the electrons to the oxonium ion in molecule 2. This shift enables the sulfuric acid to attack the carbenium ion 3 which is formed. The sulfuric acid oxidizes the resulting hydroxyanthracenone 5, which is then Protonation, protonated and the reaction starts all over ...
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Named Reaction
A name reaction is a chemical reaction named after its discoverers or developers. Among the tens of thousands of organic reactions that are known, hundreds of such reactions are well-known enough to be named after people. Well-known examples include the Grignard reaction, the Sabatier reaction, the Wittig reaction, the Claisen condensation, the Friedel-Crafts acylation, and the Diels-Alder reaction. Books have been published devoted exclusively to name reactions;Alfred Hassner, C. Stumer. ''Organic syntheses based on name reactions''. Elsevier, 2002. Li, Jie Jack. ''Name Reactions: A Collection of Detailed Reaction Mechanisms''. Springer, 2003. the Merck Index, a chemical encyclopedia, also includes an appendix on name reactions. As organic chemistry developed during the 20th century, chemists started associating synthetically useful reactions with the names of the discoverers or developers; in many cases, the name is merely a mnemonic. Some cases of reactions that were not reall ...
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