Synthesis and reactions of 5,5-dinitrobarbituric acid
โ Scribed by Abraham Langlet; Nikolaj V. Latypov; Ulf Wellmar; Patrick Goede; Jan Bergman *
- Book ID
- 104209994
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 72 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Nitration of barbituric acid at 40ยฐC gave the previously unknown 5,5-dinitrobarbituric acid (3), which readily underwent hydrolysis to dinitroacetylurea (5), which in turn could be hydrolysed in basic media to the potassium salt of dinitromethane. Alloxane was prepared in a one step procedure by thermal decomposition of 5,5dinitrobarbituric acid in hot acetic acid.
๐ SIMILAR VOLUMES
A number of interesting properties of organic azldes are known (3), and recently Robson and Malpaes have reported the synthesla and thermolysls of E-azldotropone (4). In this paper, we wish to report the synthesis and properties of 5-azldotropolones Including the synthesis of trlazolyl derivatives o