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Synthesis and characterization of new heterocyclic derivatives by oxidation of 1-amino-2-methylindoline

✍ Scribed by L. Peyrot; M. Elkhatib; J. R. Vignalou; R. Metz; F. Elomar; H. Delalu


Publisher
Journal of Heterocyclic Chemistry
Year
2001
Tongue
English
Weight
191 KB
Volume
38
Category
Article
ISSN
0022-152X

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Synthesis of 1-amino-2-methylindoline by
✍ M. Elkhatib; C. Duriche; L. Peyrot; R. Metz; H. Delalu 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 220 KB

## Abstract The synthesis of 1‐amino‐2‐methylindoline by the Raschig process was undertaken in aqueous solution. The principal side reaction that occurs in the medium is the oxidation of 1‐amino‐2‐methylindoline formed by chloramine. To increase the yield of 1‐amino‐2‐methylindoline, its oxidation

Synthesis of 1-amino-2-methylindoline by
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## Abstract The reaction between chloramine and 2‐methylindoline was studied at pH 12.89, __T__ = 40°C, and for different initial concentrations of reactants. The interaction includes two concurrent bimolecular mechanisms leading to 1‐amino‐2‐methylindoline and 2‐methylindole. The rate laws were de

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